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Thionyl Chloride → HCID 86675009, 화합물

HRID 511913
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HRID 511913 반응식
[CH2:1]([O:3][C:4]([O:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9](O)=[O:10])=[O:5])[CH3:2].S(Cl)([Cl:18])=O>C1(C)C=CC=CC=1.N1C=CC=CC=1>[CH2:1]([O:3][C:4]([O:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9]([Cl:18])=[O:10])=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 26578Carbonic acid, ethyl ester, ester with salicylic acid

생성물 1

HCID 86675009HCID 86675009, 화합물수율 81.2%

시약·촉매·용매 2

HCID 1049Pyridine촉매HCID 1140Toluene용매

실험 절차

5.9 g (28 mmol) of 2-(ethoxycarbonyloxy)benzoic acid are dissolved in 30 ml of toluene with a few drops of pyridine. 2.15 ml (29 mmol) of thionyl chloride are added dropwise and the mixture is stirred at ambient temperature for 18 h and then concentrated to dryness. The residue is precipitated from pentane. The solid is filtered off and then dried. 5.2 g of 2-(ethoxycarbonyloxy)benzoyl chloride are obtained in the form of a white solid with a yield of 80%.

후처리

  1. concentrationconcentrated to dryness
  2. customThe residue is precipitated from pentane
  3. filtrationThe solid is filtered off
  4. customdried

출처 및 근거

ORD 기록
ord-2448078ef1654767975a0b7b083fd44c
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102607B2

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