Veratraldehyde → 2-[(3,4-Dimethoxyphenyl)methylidene]-1,3-dithiolane

HRID 620065

反応式

HRID 620065 の反応式
C(OP([CH:9]1[S:14][CH2:13][CH2:12]C[S:10]1)(OCC)=O)C.[CH3:15][O:16][C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][C:24]=1[O:25][CH3:26])[CH:20]=O.[OH-].[Na+]>ClCCl.[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C>[S:14]1[CH2:13][CH2:12][S:10][C:9]1=[CH:20][C:19]1[CH:22]=[CH:23][C:24]([O:25][CH3:26])=[C:17]([O:16][CH3:15])[CH:18]=1

参加物

6

実験手順

A solution of 2-diethoxyphosphoryl-1,3-dithiane (23.4 g) and 3,4-dimethoxybenzaldehyde (16.0 g) in dichloromethane (70 ml) is added to a mixture of dichloromethane (85 ml), a 50% aqueous solution of sodium hydroxide (170 ml) and triethylbenzylammonium chloride (1.4 g). The mixture is stirred for 24 hours at room temperature. The two phases are then separated. The aqueous solution is extracted with dichloromethane (100 ml) and the combined organic solutions are washed with a 10% aqueous solution of ammonium chloride (3×100 ml) and with water (2×100 ml). The dichloromethane is dried over magnesium sulphate and evaporated in vacuo. The residue is purified by column chromatography on silica gel using chloroform as eluant. The product is dried in vacuo to constant weight to yield (1,3-dithiolan-2-ylidene)-(3,4-dimethoxyphenyl)-methane, m.p. 74°-75°.

後処理

  1. customThe two phases are then separated
  2. extractionThe aqueous solution is extracted with dichloromethane (100 ml)
  3. washthe combined organic solutions are washed with a 10% aqueous solution of ammonium chloride (3×100 ml) and with water (2×100 ml)
  4. dry with materialThe dichloromethane is dried over magnesium sulphate
  5. customevaporated in vacuo
  6. customThe residue is purified by column chromatography on silica gel
  7. customThe product is dried in vacuo to constant weight

出典と根拠

ORDレコード
ord-0f37c9248a30456a9319dc2d4ac67112
出典データセット
uspto-grants-1989_04
特許番号
US04818765

関連ノート

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