Organic catalyst with enhanced enzyme compatibility
A technology of organic catalysts and surfactants, applied in organic/inorganic compound compositions, organic cleaning compositions, skin care preparations, etc., can solve problems such as enzyme inactivation
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Embodiment 1
[0088] Example 1: 3,4-dihydro-4,4-dibenzyl-2-(3-sulfopropyl)isoquinoline Preparation of inner salt
[0089]
[0090] step 1. α, the preparation of α-dibenzyl-phenylacetonitrile (2): add benzyl cyanide (( 1), 5.0 g, 0.043 mol) and tetrahydrofuran (100 mL). Sodium hydride (60% in oil) (7.2 g, 0.1075 mol) was slowly added to the reaction over one hour. Once the addition was complete, the reaction was stirred at room temperature for 1 hour. Benzyl bromide (18.4 g; 0.043 mol) was added to the reaction and the reaction was stirred at 50°C for 18 hours. The reaction was evaporated to dryness, the residue was dissolved in toluene and washed with 1N HCl. use Na 2 SO 4 The organic phase was dried, filtered and evaporated to dryness to yield α,α-dibenzyl-phenylacetonitrile (2), weight = 7.7 g (65%).
[0091]Step 2. Preparation of 18-amino-2,2-dibenzyl-2-phenylethane (3): α,α-dibenzyl-phenylacetonitrile ((2), 7.0 g; 0.0237 mol ) was dissolved in borane-THF complex (1.1 eq...
Embodiment 2
[0094] Example 2: 3,4-dihydro-4,4-dipentyl-2-(3-sulfopropyl)isoquinoline Preparation of inner salt
[0095] The desired product was prepared according to Example 1, substituting benzyl chloride in step 1 with pentane chloride.
Embodiment 3
[0096] Example 3: 3,4-dihydro-4,4-dihexyl-2-(3-sulfopropyl)isoquinoline Preparation of inner salt
[0097] The desired product was prepared according to Example 1, replacing the benzyl chloride in step 1 with chlorohexane.
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