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Sodium Hydroxide → Carbamic acid, [2-chloro-2-(3-thienyl)ethyl]-, 1,1-dimethylethyl ester

HRID 256052
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HRID 256052 반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][CH:10]([C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)O)=[O:7])([CH3:4])([CH3:3])[CH3:2].P(Cl)(Cl)(Cl)(Cl)[Cl:18].[OH-].[Na+]>C(Cl)Cl>[C:1]([O:5][C:6]([NH:8][CH2:9][CH:10]([Cl:18])[C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24819Phosphorus pentachlorideHCID 13854065HCID 13854065, 화합물

생성물 1

HCID 13854066Carbamic acid, [2-chloro-2-(3-thienyl)ethyl]-, 1,1-dimethylethyl ester수율 55.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 12.2 g of 2-t-butoxycarbonylamino-1-(3-thienyl)ethanol [prepared as described in step (a) above] in 100 ml of absolute methylene chloride was added a solution of 10.4 g of phosphorus pentachloride in 200 ml of absolute methylene chloride at 0° to -5° C. After the addition, the reaction mixture was stirred for 10 minutes. To the reaction mixture was added a 4N aqueous solution of sodium hydroxide, and the mixture was stirred for 5 minutes. The methylene chloride layer was separated, washed with large amount of water and dried over anhydrous magnesium sulfate, and the solvent was evaporated off. The residue was subjected to silica gel column chromatography using a 1:4 by volume mixture of ethyl acetate and cyclohexane as eluent, to yield 7.3 g of the title compound melting at 63°-65° C.

후처리

  1. additionAfter the addition
  2. stirringthe mixture was stirred for 5 minutes
  3. customThe methylene chloride layer was separated
  4. washwashed with large amount of water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated off
  7. additionby volume mixture of ethyl acetate and cyclohexane as eluent

출처 및 근거

ORD 기록
ord-e78819c6aac74ed4a4d4ab8edcbe1a30
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04699905

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