3-Ethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid → 1-(3-Ethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone

HRID 1013441ノート

反応式

HRID 1013441 の反応式
[CH2:1]([C:3]1[S:7][C:6]([C:8]([OH:10])=O)=[C:5]2[CH2:11][CH2:12][C:13]([CH3:16])([CH3:15])[CH2:14][C:4]=12)[CH3:2].[CH3:17][Li]>C(OCC)C>[CH2:1]([C:3]1[S:7][C:6]([C:8](=[O:10])[CH3:17])=[C:5]2[CH2:11][CH2:12][C:13]([CH3:16])([CH3:15])[CH2:14][C:4]=12)[CH3:2]

参加物

4

実験手順

To a solution of 3-ethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (2.10 g, 8.81 mmol) in diethyl ether (100 mL), a solution of methyllithium (11 mL, 1.6 M solution in diethyl ether) is added at rt. The pale yellow solution is stirred at rt for 15 min before another portion of methyllithium (2 mL) is added. Stirring is continued for 15 min, a further portion of methyllithium (1 mL) is added, and the mixture is again stirred for 15 min at rt. The reaction is quenched with water. The organic layer is separated, washed once more with water, dried over MgSO4 and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 7:3 to give 1-(3-ethyl-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone (1.65 g) as a pale yellow solid; LC-MS: tR=1.00 min; [M+1]=237.15; 1H NMR (CDCl3): δ 3.03 (t, J=7.0 Hz, 2H), 2.73 (q, J=7.6 Hz, 2H), 2.47 (s, 3H), 2.31 (s, 2H), 1.55 (t, J=7.0 Hz, 2H), 1.28 (t, J=7.6 Hz, 3H), 0.97 (s, 6H).

後処理

  1. additionis added
  2. stirringthe mixture is again stirred for 15 min at rt
  3. customThe reaction is quenched with water
  4. customThe organic layer is separated
  5. washwashed once more with water
  6. dry with materialdried over MgSO4
  7. customevaporated
  8. customThe crude product is purified by CC on silica gel eluting with heptane:EA 7:3

出典と根拠

ORDレコード
ord-5610634bf46c4e48980b1613aef5f9db
出典データセット
uspto-grants-2011_07
特許番号
US07981924B2

反応ノート

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