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Chlorodifluoromethane → Methyl 5-(difluoromethoxy)-2-methylbenzoate

HRID 524321
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HRID 524321 반응식
Cl[CH:2]([F:4])[F:3].[OH:5][C:6]1[CH:7]=[CH:8][C:9]([CH3:16])=[C:10]([CH:15]=1)[C:11]([O:13][CH3:14])=[O:12].[OH-].[Na+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O1CCOCC1>[F:3][CH:2]([F:4])[O:5][C:6]1[CH:7]=[CH:8][C:9]([CH3:16])=[C:10]([CH:15]=1)[C:11]([O:13][CH3:14])=[O:12]
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참가 물질

6

반응물 3

HCID 6372ChlorodifluoromethaneHCID 14798Sodium HydroxideHCID 13929055Methyl 5-hydroxy-2-methylbenzoate

생성물 1

HCID 53418071Methyl 5-(difluoromethoxy)-2-methylbenzoate

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매HCID 312751,4-Dioxane용매

실험 절차

Chloro(difluoro)methane is introduced with vigorous stirring for 90 minutes into a mixture of 50 g methyl 5-hydroxy-2-methylbenzoate (see below), 1.21 g tetrabutylammonium bromide, 52 g aqueous sodium hydroxide solution (50% by weight) and 500 ml dioxane. The reaction mixture is filtered and the filtrate is adjusted to pH 1-2 with 1n aqueous hydrochloric acid. The mixture is extracted with EA three times, the combined organics are dried over MgSO4, and the solvent is removed under reduced pressure. The resulting crude product is purified by filtration over a column (silica gel and PE) yielding methyl 5-(difluoromethoxy)-2-methylbenzoate, which is used for the next step without further purification.

후처리

  1. filtrationThe reaction mixture is filtered
  2. extractionThe mixture is extracted with EA three times
  3. dry with materialthe combined organics are dried over MgSO4
  4. customthe solvent is removed under reduced pressure
  5. filtrationThe resulting crude product is purified by filtration over a column (silica gel and PE)

출처 및 근거

ORD 기록
ord-c96ece91850e4d6daac90266775a072c
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340522B2

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