Nitromethane → 4-Nitro-3-(4-trifluoromethylphenyl)butanoic acid ethyl ester

HRID 464733ノート

反応式

HRID 464733 の反応式
[CH2:1]([O:3][C:4](=[O:17])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][CH:8]=1)[CH3:2].[N+:18]([CH3:21])([O-:20])=[O:19].CN(C)C(=N)N(C)C>C(OCC)C.Cl>[CH2:1]([O:3][C:4](=[O:17])[CH2:5][CH:6]([C:7]1[CH:12]=[CH:11][C:10]([C:13]([F:15])([F:16])[F:14])=[CH:9][CH:8]=1)[CH2:21][N+:18]([O-:20])=[O:19])[CH3:2]

参加物

6

反応物 3

HCID 6375NitromethaneHCID 664601,1,3,3-TetramethylguanidineHCID 53662772Ethyl 3-[4-(trifluoromethyl)phenyl]prop-2-enoate

生成物 1

HCID 539494754-Nitro-3-(4-trifluoromethylphenyl)butanoic acid ethyl ester

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 3283Diethyl Ether溶媒

実験手順

A mixture of 300 g of 4-trifluoromethylcinnamic acid ethyl ester, 500 g of nitromethane, and 39 g of tetramethylguanidine is allowed to stir for 72 hours. The solution is diluted with diethyl ether and aqueous hydrochloric acid solution (1 N, 1 liter) is added. The organic layer is separated, dried over anhydrous magnesium sulfate and evaporated to give 4-nitro-3-(4-trifluoromethylphenyl)butanoic acid ethyl ester.

後処理

  1. additionis added
  2. customThe organic layer is separated
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customevaporated

出典と根拠

ORDレコード
ord-26d2310af9124e53b97b6379ce7782c0
出典データセット
uspto-grants-1985_10
特許番号
US04548947

反応ノート

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