Lithium hydroxide, monohydrate → 2-Nitro-terephthalic acid 1-tert-butyl ester
반응식
C[O:2][C:3](=[O:20])[C:4]1[CH:16]=[CH:15][C:7]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])=[C:6]([N+:17]([O-:19])=[O:18])[CH:5]=1.O.[OH-].[Li+]>C1COCC1.O>[C:11]([O:10][C:8](=[O:9])[C:7]1[CH:15]=[CH:16][C:4]([C:3]([OH:20])=[O:2])=[CH:5][C:6]=1[N+:17]([O-:19])=[O:18])([CH3:14])([CH3:12])[CH3:13]참가 물질
실험 절차
2-Nitro-terephthalic acid 1-tert-butyl ester 4-methyl ester (21.49 mmol) was dissolved in THF (143 mL) and treated with lithium hydroxide monohydrate (1.35 g, 32.24 mmol) in water (97 mL). The reaction was stirred at room temperature for 2 hours then partially evaporated, cooled with an ice/water bath and treated with 1N HCl dropwise (35 mL). Precipitation of a solid occurred. The mixture was then extracted with DCM (150 mL and 2×50 mL) The aqueous phase was further treated with 1N HCl (10 mL) and extracted with DCM (2×50 mL). The combined organic layers were then washed with water and finally with brine. After drying over sodium sulphate and evaporation, 5.34 g of title compound were obtained as a reddish solid in 93% overall yield.
후처리
- customthen partially evaporated
- temperaturecooled with an ice/water bath
- additiontreated with 1N HCl dropwise (35 mL)
- customPrecipitation of a solid
- extractionThe mixture was then extracted with DCM (150 mL and 2×50 mL) The aqueous phase
- additionwas further treated with 1N HCl (10 mL)
- extractionextracted with DCM (2×50 mL)
- washThe combined organic layers were then washed with water and finally with brine
- dry with materialAfter drying over sodium sulphate and evaporation
출처 및 근거
- ORD 기록
- ord-77c07ae75c874d7bae8703357784eea0
- 출처 데이터셋
- uspto-grants-2015_07
- 특허 번호
- US09085558B2
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