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Sodium borohydride → Tert-butyl 4-(1-aminopropyl)-2-nitrobenzoate

HRID 554824
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HRID 554824 반응식
[N+:1]([C:4]1[CH:16]=[C:15]([C:17](=O)[CH2:18][CH3:19])[CH:14]=[CH:13][C:5]=1[C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])([O-:3])=[O:2].[BH4-].[Na+].O.[NH3:24]>N.C(O)C.C(O[Ti](OC(C)C)(OC(C)C)OC(C)C)(C)C>[NH2:24][CH:17]([C:15]1[CH:14]=[CH:13][C:5]([C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])=[C:4]([N+:1]([O-:3])=[O:2])[CH:16]=1)[CH2:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 4311764Sodium borohydrideHCID 12896473Azane;hydrateHCID 66935244Tert-butyl 2-nitro-4-propionylbenzoate

생성물 1

HCID 67461906Tert-butyl 4-(1-aminopropyl)-2-nitrobenzoate

시약·촉매·용매 2

HCID 178460666HCID 178460666, 화합물촉매
HCID 22020343
Ethanol, reaction products with ammonia, distn. residues
용매

실험 절차

Tert-butyl 2-nitro-4-propionylbenzoate (9.2 g) was suspended in 2N ammonia/ethanol solution (81 ml), then tetraisopropoxytitanium (18.7 ml) was added at room temperature and the mixture was stirred at that temperature for 6 hours. Next, sodium borohydride (1.8 g) was added to the mixture, and the resulting mixture was stirred at that temperature for 16 hours. Then 2.1N ammonia water (81 ml) and Celite (9g) were added to the reaction solution and the inspluble materials were filtered off and washed with water and ethyl acetate. The filtrate was concentrated in vacuo, then a 5N aqueous sodium hydroxide solution and ethyl acetate were added to the obtained residue. The separated organic layer was concentrated in vacuo, then the obtained residue was purified by silica gel column chromatography to obtain the title compound (7.6 g) as an oily substance.

후처리

  1. stirringthe resulting mixture was stirred at that temperature for 16 hours
  2. filtrationthe inspluble materials were filtered off
  3. washwashed with water and ethyl acetate
  4. concentrationThe filtrate was concentrated in vacuo
  5. additiona 5N aqueous sodium hydroxide solution and ethyl acetate were added to the obtained residue
  6. concentrationThe separated organic layer was concentrated in vacuo
  7. customthe obtained residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-9fdd327512614da6b1a8fe56fa00f978
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08049006B2

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