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Preparation technique of 1,6-dimethoxynaphthalene

A dimethoxynaphthalene, a preparation technology, applied in 1 field, can solve the problems such as difficult recovery of solvent methanol, high cost, expensive acetone, etc.

Active Publication Date: 2009-07-01
NANTONG BAISHENG CHEM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Methylation in methanol-NaOH-water solution, the solvent methanol is not easy to recover
in K 2 CO 3 —Methylation of acetone mixture, K 2 CO 3 , Acetone is more expensive and the cost is higher

Method used

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  • Preparation technique of 1,6-dimethoxynaphthalene
  • Preparation technique of 1,6-dimethoxynaphthalene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Add 20g of 1,6-dihydroxynaphthalene, 102g of petroleum ether (boiling point 60-90°C), 99g of NaOH aqueous solution with a NaOH content of 16%, 1g of hydrosulfite, 0.5g of tetramethylammonium chloride, and drop Add 26g Me 2 SO 4 (15 minutes to finish dripping). Heated to 55-60°C, reacted for 1h. Add 49g NaOH content then and be the NaOH aqueous solution of 16%, dropwise add 20g Me 2 SO 4 (After 15 minutes of dripping), add to 55-60°C, and react for 4 hours.

[0024] Then separate the liquid in a separatory funnel while it is hot, take out the upper oil layer, pour it into a beaker, stir it magnetically, cool it down to 0-5°C in an ice-water bath (keep for 1h), and then filter to obtain yellow crystals of 1,6-dimethoxy naphthalene. Yield 70%, purity 98.6%.

Embodiment 2

[0026] Add 20g 1,6-dihydroxynaphthalene, 150g petroleum ether (boiling point 60-90°C), 115g NaOH aqueous solution with 16% NaOH content, 0.5g hydrosulfite, 1g tetramethylammonium chloride, drop Add 32gMe 2 SO 4 (15 minutes to finish dripping). Heated to 55-60°C, reacted for 0.5h. Add 55g NaOH content then and be the NaOH aqueous solution of 16%, dropwise add 24g Me 2 SO 4 (After 15 minutes of dripping), add to 55-60°C, and react for 7 hours.

[0027] Then separate the liquid in a separatory funnel while it is hot, take out the upper oil layer, pour it into a beaker, stir it magnetically, cool it down to 0-5°C in an ice-water bath (keep for 1h), and then filter to obtain yellow crystals of 1,6-dimethoxy naphthalene. Yield 72%, purity 98.3%.

Embodiment 3

[0029] Operate in the same manner as in Example 2, but replace tetramethylammonium chloride with 0.5g octadecyltrimethylammonium chloride, as a result, yellow crystal 1,6-dimethoxynaphthalene is obtained, yield 71.2%, purity 98.1% %.

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Abstract

The invention puts forward a novel process for synthesizing 1,6-dimethoxynaphthalene. The process comprises the steps of adding sodium hydrosulfite for preventing oxidation to a medium of petroleum ether and NaOH aqueous solution, adding quaternary ammonium salt as a phase transition catalyst, using dimethyl sulfate to methylate 1,6-dihydroxynaphthlene, adding NaOH aqueous solution and dimethyl sulfate by stages, performing reaction at a temperature between 50 and 60 DEG C and preparing the 1,6-dimethoxynaphthalene. In a first stage, the weight ratio of petroleum ether, the NaOH aqueous solution, the sodium hydrosulfite, the quaternary ammonium salt and the dimethyl sulfate to the 1,6-dimethoxynaphthalene is 4.5-8:1, 4.6-6:1, 0.02-0.06:1, 0.02-0.05:1 and 1.2-1.8:1 respectively; the time of dripping the dimethyl sulfate is 10 to 60 minutes; and in a second stage, the weight ratio of the added NaOH aqueous solution and the dimethyl sulfate to the 1,6-dimethoxynaphthalene is 2.3-3:1 and 0.88-1.2:1 respectively. The method has the advantages that reaction conditions are easy to control; the petroleum ether can be recovered and indiscriminately used; and the 1,6-dimethoxynaphthalene is high in purity and does not need to be refined by use of solvents.

Description

Technical field: [0001] The invention belongs to the methylation method of naphthol compounds, and particularly proposes a preparation method of 1,6-dimethoxynaphthalene. Background technique: [0002] 1,6-dimethoxynaphthalene is an important organic intermediate used in the synthesis of medicines, pesticides, dyes and other functional materials, and has a good market prospect. [0003] From 1,6-dihydroxynaphthalene, after dimethyl sulfate dimethylation, 1,6-dimethoxynaphthalene can be prepared. The reaction medium can be NaOH aqueous solution, methanol-NaOH-water solution, K 2 CO 3 - Acetone mixture. Methylation in NaOH aqueous solution, dimethyl sulfate is easily hydrolyzed, 1,6-dihydroxynaphthalene is easily oxidized, and the yield is low. Methylation in methanol-NaOH-water solution, the solvent methanol is not easy to recover. in K 2 CO 3 —Methylation of acetone mixture, K 2 CO 3 , Acetone is more expensive and the cost is higher. In the above several synthetic...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C43/257C07C41/16
Inventor 袁仲飞张天永
Owner NANTONG BAISHENG CHEM
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