반응식
[BH4-].[Na+].[CH2:3]1[CH2:7][O:6][CH2:5][CH2:4]1.[Br:8][C:9]1[CH:14]=[CH:13]C=[CH:11][C:10]=1CCC(O)=O.B(F)(F)F.CCOCC>CC(OC)(C)C.O>[Br:8][C:9]1[CH:14]=[CH:13][C:5]([CH2:4][CH2:3][CH2:7][OH:6])=[CH:11][CH:10]=1참가 물질
반응 조건
- 온도
- 25 °C
실험 절차
Sodium borohydride (119.12 g) and THF (5 L) were charged into reactor 1 and temperature adjusted to −20° C. 3-(bromophenyl)propionic acid (1 kg) was charged into reactor 2 with THF (3 L) and stirred at 25° C. until all the solids dissolved. This solution in reactor 2 was transferred to reactor 1 maintaining reactor 1 contents at <0° C. BF3.Et2O (991.4 g) was slowly added into reactor 1 maintaining reactor 1 contents at −20 to −10° C. After addition, the mixture was stirred at −20 to −10° C. for 1 h. The reaction is analysed for completion (3-(bromophenyl)propionic acid <2.5%). Water (2 L) was slowly added into reactor 1 to quench the reaction. (gas evolution). MTBE (5 L) was charged into reactor 1 and phases separation was carried out. The upper layer was collected and lower layer was washed with MTBE (5 L). The upper layer was collected and combined with the layer from the previous step. Adjusted pH value of the organic layer to 8-9 by adding 1N NaOH solution. The organic layer was washed with saturated NaCl solution (2 L) and the upper layer was collected. The organic layer was evaporated down to a colourless oil.
후처리
- customadjusted to −20° C
- dissolutiondissolved
- customThis solution in reactor 2 was transferred to reactor
- customat <0° C
- additionAfter addition
- stirringthe mixture was stirred at −20 to −10° C. for 1 h
- customto quench
- customthe reaction
- custom1 and phases separation
- customThe upper layer was collected
- washlower layer was washed with MTBE (5 L)
- customThe upper layer was collected
- additionAdjusted pH value of the organic layer to 8-9 by adding 1N NaOH solution
- washThe organic layer was washed with saturated NaCl solution (2 L)
- customthe upper layer was collected
- customThe organic layer was evaporated down to a colourless oil
출처 및 근거
- ORD 기록
- ord-34040895c7734d0f8dcdc8093bf0d886
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08198285B2
연결된 노트
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