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Benzyl chloroformate → Benzyl 4-(2-hydroxy-4-methoxybenzoyl)piperidine-1-carboxylate

HRID 647283
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HRID 647283 반응식
[OH:1][C:2]1[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=[CH:12][C:3]=1[C:4]([CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5].C(=O)(O)[O-].[Na+].Cl[C:24]([O:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:25]>ClCCl>[OH:1][C:2]1[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=[CH:12][C:3]=1[C:4]([CH:6]1[CH2:7][CH2:8][N:9]([C:24]([O:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[O:25])[CH2:10][CH2:11]1)=[O:5]
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참가 물질

5

반응물 3

HCID 10387Benzyl chloroformateHCID 516892Sodium BicarbonateHCID 13076390(2-Hydroxy-4-methoxyphenyl)(piperidin-4-yl)methanone

생성물 1

HCID 13076396Benzyl 4-(2-hydroxy-4-methoxybenzoyl)piperidine-1-carboxylate수율 76.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a stirred, ice-cooled mixture of 36.1 g of 4-(2-hydroxy-4-methoxybenzoyl)piperidine, 16.3 g of sodium bicarbonate and 350 ml of dichloromethane, was added dropwise 22.9 ml of benzyl chloroformate in dichloromethane. After the addition was complete, the mixture was stirred at ambient temperature for 1.5 hrs, filtered and the filtrate concentrated to an oil. The oil crystallized. The crystals were collected, washed with hexane and dried to yield 42.4 g (76.5%) of product. Recrystallization from isopropanol gave the analytical sample, mp, 89°-91°.

후처리

  1. temperatureTo a stirred, ice-cooled
  2. additionAfter the addition
  3. filtrationfiltered
  4. concentrationthe filtrate concentrated to an oil
  5. customThe oil crystallized
  6. customThe crystals were collected
  7. washwashed with hexane
  8. customdried

출처 및 근거

ORD 기록
ord-41ddc60443c1463f9902045298e254ab
출처 데이터셋
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04408053

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