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1,4-Dibromobutane → Ethyl 1-acetylcyclopentane-1-carboxylate

HRID 1935983
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HRID 1935983 반응식
C[O-].[Na+].[C:4]([O:10][CH2:11][CH3:12])(=[O:9])[CH2:5][C:6]([CH3:8])=[O:7].Br[CH2:14][CH2:15][CH2:16][CH2:17]Br>CN(C=O)C>[CH2:11]([O:10][C:4]([C:5]1([C:6](=[O:7])[CH3:8])[CH2:17][CH2:16][CH2:15][CH2:14]1)=[O:9])[CH3:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80561,4-DibromobutaneHCID 8868Ethyl AcetoacetateHCID 10942334Sodium Methoxide

생성물 1

HCID 13050135Ethyl 1-acetylcyclopentane-1-carboxylate수율 78.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
90 °C

실험 절차

27.2 g (0.4 mol) of sodium methoxide are initially introduced into 300 ml of DMF at approx. 40° C. and stirred. A mixture of 26 g (0.2 mol) of ethyl acetoacetate and 43 g (0.2 mol) of 1,4-dibromobutane is slowly added dropwise to this suspension and the reaction mixture is stirred for approx. 24 hours at this temperature. Towards the end of the reaction, the temperature may optionally be raised to 90° C. for a further hour. The precipitated sodium bromide is filtered out, the DMF removed and the residue fractionated. 29 g (78%) of 1-acetyl-1-cyclopentanecarboxylic acid ethyl ester are obtained. Bp.: 136° C. (1500 Pa); IR: 1745 cm−1 (C═O, ester), 1713 cm−1 (C═O, ketone); MS: m/e=142 (M−42), 114, 101, 96, 86, 67, 43.

후처리

  1. additionis slowly added dropwise to this suspension
  2. stirringthe reaction mixture is stirred for approx. 24 hours at this temperature
  3. customTowards the end of the reaction
  4. filtrationThe precipitated sodium bromide is filtered out
  5. customthe DMF removed

출처 및 근거

ORD 기록
ord-4a922325092e4776a90a25b6eda0b0b0
출처 데이터셋
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06388104B1

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