Method for preparing normal aldehyde based on olefin two-phase hydroformylation high selectivity of polyether quaternary ammonium salt ionic liquid
A quaternary ammonium salt ion, high-selectivity technology, applied in the field of two-phase hydroformylation of olefins to prepare n-formaldehyde with high selectivity, can solve the problems of shortened service life, reduced stability, low catalytic activity and the like
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Embodiment 1
[0020] Rh(acac)(CO) 2 / BISBI-(SO 3 Na) 2 (1) / [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] / 1-octene system under the two-phase hydroformylation reaction (l=m=2)
[0021] Under an inert atmosphere, add Rh(acac)(CO) to a stainless steel autoclave 2 , BISBI-(SO 3 Na) 2 (1), [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] and 1-octene, the ratio is: BISBI-(SO 3 Na) 2 (1) / Rh(acac)(CO) 2 =5:1 (molar ratio), 1-octene / Rh(acac)(CO) 2 =1000:1 (molar ratio), [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] / Rh(acac)(CO) 2 =300:1 (molar ratio), then use synthesis gas (H 2 / CO=1:1) pressurize to 5.0MPa, reaction temperature 100°C, reaction time 0.5 hours, then rapidly cool to room temperature, vent the syngas and open the kettle, the ionic liquid phase in the lower layer solidifies, through the ionic liquid phase and the organic phase Liquid / solid two-phase separation realizes the recovery of rhodium catalyst, and n-heptane can also be...
Embodiment 2
[0023] Rh(acac)(CO) 2 / BINA-(SO 3 Na) 2 (2) / [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] / 1-octene two-phase hydroformylation reaction (q=p=1; l=m=2)
[0024] Under an inert atmosphere, add Rh(acac)(CO) to a stainless steel autoclave 2 , BINA-(SO 3 Na) 2 (2), [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] and 1-octene in a ratio of: BINA-(SO 3 Na) 2 (2) / Rh(acac)(CO) 2 =5:1 (molar ratio), 1-octene / Rh(acac)(CO) 2 =5000:1 (molar ratio), [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] / Rh(acac)(CO) 2 =300:1 (molar ratio), then use synthesis gas (H 2 / CO=1:1) pressurize to 5.0MPa, reaction temperature 100°C, reaction time 0.5 hours, then rapidly cool to room temperature, vent the syngas and open the kettle, the ionic liquid phase in the lower layer solidifies, through the ionic liquid phase and the organic phase Liquid / solid two-phase separation realizes the recovery of rhodium catalyst, and n-heptane can also be added for ex...
Embodiment 3
[0026] Rh(acac)(CO) 2 / Xantphos-(SO 3 Na) 2 (3) / [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] / 1-octene system under the two-phase hydroformylation reaction (l=m=2)
[0027] Under an inert atmosphere, add Rh(acac)(CO) to a stainless steel autoclave 2 , Xantphos-(SO 3 Na) 2 (3), [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] and 1-octene in a ratio of: Xantphos-(SO 3 Na) 2 (3) / Rh(acac)(CO) 2 =5:1 (molar ratio), 1-octene / Rh(acac)(CO) 2 =1000:1 (molar ratio), [Ph(OCH 2 CH 2 ) 16 N + (C 2 h 5 ) 3 ][CH 3 SO 3 - ] / Rh(acac)(CO) 2 =300:1 (molar ratio), then use synthesis gas (H 2 / CO=1:1) pressurize to 5.0MPa, reaction temperature 100°C, reaction time 0.5 hours, then rapidly cool to room temperature, vent the syngas and open the kettle, the ionic liquid phase in the lower layer solidifies, through the ionic liquid phase and the organic phase Liquid / solid two-phase separation realizes the recovery of rhodium catalyst, and n-heptane ca...
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