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Potassium Bromide → Methyl 2-bromo-2-(3,5-dichlorophenyl)acetate

HRID 1666300
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HRID 1666300 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9](OS(C)(=O)=O)[C:10]([O:12][CH3:13])=[O:11])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[Br-:19].[K+]>CN(C)C=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([Br:19])[C:10]([O:12][CH3:13])=[O:11])[CH:5]=[C:6]([Cl:8])[CH:7]=1
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참가 물질

4

반응물 2

HCID 253877Potassium BromideHCID 86629543HCID 86629543, 화합물

생성물 1

HCID 77174840Methyl 2-bromo-2-(3,5-dichlorophenyl)acetate수율 102.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of methyl 2-(3,5-dichlorophenyl)-2-mesyloxyacetate (8.2 g) in dimethylformamide (30 ml) was treated with potassium bromide (4.0 g) at 50° C. for 1.5 hours. The reaction mixture was partitioned between water (200 ml) and ethyl acetate (300 ml). The organic phase was separated and washed twice with water (2×200 ml) and finally with saturated brine solution (200 ml). The ethyl acetate solution was dried and concentrated to dryness giving crude methyl 2-(3,5-dichlorophenyl)-2-bromoacetate (8 g). Filtration through a column of silica gel using dichloromethane as eluent gave the pure substance as an oil (7.4 g).

후처리

  1. customThe reaction mixture was partitioned between water (200 ml) and ethyl acetate (300 ml)
  2. customThe organic phase was separated
  3. washwashed twice with water (2×200 ml) and finally with saturated brine solution (200 ml)
  4. dry with materialThe ethyl acetate solution was dried
  5. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-602b5c95884249648066255bcff9c84b
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044067B2

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