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

HRID 1914249
ノート
印刷プレビュー

反応式

HRID 1914249 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 74236Tetrabutylammonium Bromide触媒HCID 312751,4-Dioxane溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-bb5f7a414fdf47d9a49fa8c5864df4b8
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08609848B2

反応ノート

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