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Dimethylformamide → HCID 17862638, 화합물

HRID 1766937
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HRID 1766937 반응식
[CH2:1]([O:4][C:5]([O:7][CH2:8][C:9]1[CH:17]=[CH:16][C:15]([C:18]#[N:19])=[CH:14][C:10]=1[C:11](O)=[O:12])=[O:6])[CH:2]=[CH2:3].CN(C)C=O.C(Cl)(=O)C([Cl:28])=O>ClCCl.C1(C)C=CC=CC=1>[CH2:1]([O:4][C:5]([O:7][CH2:8][C:9]1[CH:17]=[CH:16][C:15]([C:18]#[N:19])=[CH:14][C:10]=1[C:11]([Cl:28])=[O:12])=[O:6])[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 17862562HCID 17862562, 화합물

생성물 1

HCID 17862638HCID 17862638, 화합물

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6344Dichloromethane용매

실험 절차

2-[(Allyloxycarbonyl)oxymethyl]-5-cyanobenzoic acid (1.6 g, 6.12 mmol) obtained from Example 33-(2) was dissolved in dichloromethane (40 ml), and N,N-dimethylformamide (0.05 ml) and oxalyl chloride (2 g) were added thereto. The mixture was stirred at room temperature for 1 hour, then diluted with toluene, and the solvent was distilled off under reduced pressure to give crude 2-[(allyloxycarbonyl)oxymethyl]-5-cyanobenzoyl chloride.

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후처리

  1. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-0069bc074c1b44c2bcf5a05afc65a48c
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07230023B2

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