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HCID 20452409, 화합물 → HCID 20452406, 화합물

HRID 1462937
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HRID 1462937 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:21]=[CH:22][C:23]=1[O:24][CH3:25])[C:12]([NH:14][CH2:15][CH2:16][CH2:17][C:18](O)=[O:19])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(OC(=O)C)(=O)C>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:21]=[CH:22][C:23]=1[O:24][CH3:25])[C:12]([N:14]1[CH2:15][CH2:16][CH2:17][C:18]1=[O:19])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 20452409HCID 20452409, 화합물

생성물 1

HCID 20452406HCID 20452406, 화합물

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

2.0 g of 4-[(3-benzyloxy-4-methoxybenzoyl)amino]butyric acid are heated to reflux for 1 hour in 10 ml of acetic acid anhydride. After evaporation of the acetic acid anhydride, the residue is stirred at room temperature with diethyl ether. The mixture is filtered and the filter residue is washed with diethyl ether. There is obtained 1-(3-benzyloxy-4-methoxybenzoyl)-2-pyrrolidinone of melting point 92°-92° C.

후처리

  1. customAfter evaporation of the acetic acid anhydride
  2. filtrationThe mixture is filtered
  3. washthe filter residue is washed with diethyl ether

출처 및 근거

ORD 기록
ord-3be0b0964e7542e7b9ebb7ae002aa14d
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461906

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