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Phenolate Sodium → HCID 53993923, 화합물

HRID 2073410
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반응식

HRID 2073410 반응식
Cl[C:2]([Cl:12])=[CH:3][C:4]([CH2:10][CH3:11])([CH3:9])[CH2:5][CH2:6][CH2:7][CH3:8].[C:13]1([O-:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[Na+]>CN(C)C=O.C(Cl)Cl>[Cl:12][CH:2]=[C:3]([O:19][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:4]([CH2:10][CH3:11])([CH3:9])[CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 4445035Phenolate SodiumHCID 13849834HCID 13849834, 화합물

생성물 1

HCID 53993923HCID 53993923, 화합물수율 65.3%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매

실험 절차

626 g (3 moles) of 1,1-dichloro-3-ethyl-3-methyl-1-heptene and 676 g (6 moles) of sodium phenolate are heated under relfux in 3 l of dimethylformamide for 16 hours. The mixture is diluted with methylene chloride and extracted by shaking several times with 2N aqueous sodium hydroxide solution. After drying and evaporating on a rotary evaporator, 666 g of crude product remain. Distillation at boiling point0.1 100°-110° C. gives 523 g (65% of theory) of 1-chloro-3-ethyl-3-methyl-2-phenoxy-hept-1-ene.

후처리

  1. extractionextracted
  2. customAfter drying
  3. customevaporating on a rotary evaporator, 666 g of crude product
  4. distillationDistillation
  5. customat boiling point0.1 100°-110° C.

출처 및 근거

ORD 기록
ord-bd83b4e780b64b329099077e5f87a30f
출처 데이터셋
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04917720

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