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Thionyl Chloride → HCID 21510426, 화합물

HRID 1576954
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반응식

HRID 1576954 반응식
O[CH2:2][CH:3]([O:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:4](=[O:9])[C:5]([CH3:8])([CH3:7])[CH3:6].S(Cl)([Cl:19])=O>C(Cl)Cl>[Cl:19][CH2:2][CH:3]([O:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:4](=[O:9])[C:5]([CH3:8])([CH3:7])[CH3:6]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 21510427HCID 21510427, 화합물

생성물 1

HCID 21510426HCID 21510426, 화합물수율 77.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1-Hydroxy-2-phenoxy-4,4-dimethyl-pentan-3-one (111.1 g, 0.5 mol) is dissolved in 500 ml of methylene chloride. Thionyl chloride (62 g, 0.52 mol) is added dropwise to the solution at room temperature. The start of the reaction can be accelerated by gentle warming. After a reaction time of two hours at room temperature, the solvent is distilled off in vacuo and the oily residue is degassed in a high vaccum to afford 93.0 g (77% of theory) of 1-chloro-4,4-dimethyl-2-phenoxy-pentan-3-one as an oil having a refractive index of nD20 = 1.5081 and a boiling point of (0.4 mm Hg)/110°C.

후처리

  1. customThe start of the reaction
  2. distillationAfter a reaction time of two hours at room temperature, the solvent is distilled off in vacuo
  3. customthe oily residue is degassed in a high vaccum

출처 및 근거

ORD 기록
ord-f28347fb705c4ccebb12293f5a2fa7dc
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03983240

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