Hydrochloric Acid → 3-{4-[3-(5,5-Dimethyl-3-trifluoromethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-3-oxo-propenyl]-2-ethyl-6-methyl-phenyl}-acrylic acid ethyl ester

HRID 1665957ノート

反応式

HRID 1665957 の反応式
[CH3:1][C:2]1([CH3:18])[CH2:17][CH2:16][C:5]2=[C:6]([C:13](=[O:15])[CH3:14])[S:7][C:8]([C:9]([F:12])([F:11])[F:10])=[C:4]2[CH2:3]1.[CH2:19]([C:21]1[CH:26]=[C:25]([CH:27]=O)[CH:24]=[C:23]([CH3:29])[C:22]=1[CH:30]=[CH:31][C:32]([OH:34])=[O:33])[CH3:20].Cl.[CH2:36](O)[CH3:37]>C(O)(C)C.C([O-])(O)=O.[Na+]>[CH2:36]([O:34][C:32](=[O:33])[CH:31]=[CH:30][C:22]1[C:23]([CH3:29])=[CH:24][C:25]([CH:27]=[CH:14][C:13]([C:6]2[S:7][C:8]([C:9]([F:12])([F:10])[F:11])=[C:4]3[CH2:3][C:2]([CH3:18])([CH3:1])[CH2:17][CH2:16][C:5]=23)=[O:15])=[CH:26][C:21]=1[CH2:19][CH3:20])[CH3:37]

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 575089061-(5,5-Dimethyl-3-trifluoromethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanoneHCID 765393093-(2-Ethyl-4-formyl-6-methyl-phenyl)-acrylic acid

生成物 1

HCID 671883473-{4-[3-(5,5-Dimethyl-3-trifluoromethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-3-oxo-propenyl]-2-ethyl-6-methyl-phenyl}-acrylic acid ethyl ester

試薬・触媒・溶媒 2

HCID 3776Isopropanol溶媒HCID 516892Sodium Bicarbonate溶媒

反応条件

温度
65 °C

実験手順

A solution of 1-(5,5-dimethyl-3-trifluoromethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone (500 mg, 1.81 mmol) and 3-(2-ethyl-4-formyl-6-methyl-phenyl)-acrylic acid (395 mg, 1.81 mmol) in ethanol (25 mL) is treated with 5 N HCl in isopropanol (15 mL). The orange brown reaction mixture is stirred at 65° C. for 64 h. The mixture is diluted with sat. aq. NaHCO3 solution and extracted twice with EA. The organic extracts are washed with sat. NaHCO3 solution, dried over MgSO4, filtered and the solvent of the filtrate is evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 9:1 to give 3-{4-[3-(5,5-dimethyl-3-trifluoromethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-3-oxo-propenyl]-2-ethyl-6-methyl-phenyl}-acrylic acid ethyl ester (634 mg, contains traces of the corresponding isopropyl ester) as a colourless oil; LC-MS: tR=1.32 min, [M+1]=505.04.

後処理

  1. extractionextracted twice with EA
  2. washThe organic extracts are washed with sat. NaHCO3 solution
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customthe solvent of the filtrate is evaporated
  6. customThe crude product is purified by CC on silica gel eluting with heptane:EA 9:1

出典と根拠

ORDレコード
ord-7fc677ff6c9247cab480c0dfed2b6fc3
出典データセット
uspto-grants-2011_10
特許番号
US08039644B2

反応ノート

読み込み中…