Seratrodast → 6-(6-Methoxycarbonyl-1-phenylhexyl)-2,3,5-trimethylbenzoquinone

HRID 864710

反応式

HRID 864710 の反応式
[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]([C:16]1[C:21](=[O:22])[C:20]([CH3:23])=[C:19]([CH3:24])[C:18](=[O:25])[C:17]=1[CH3:26])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)([OH:3])=[O:2].[N+](=[CH2:29])=[N-].CCOCC>CCOCC>[CH3:29][O:2][C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]([C:16]1[C:21](=[O:22])[C:20]([CH3:23])=[C:19]([CH3:24])[C:18](=[O:25])[C:17]=1[CH3:26])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)=[O:3]

参加物

4

反応物 2

HCID 2449SeratrodastHCID 21186548Diazomethane diethylether

生成物 1

HCID 98640816-(6-Methoxycarbonyl-1-phenylhexyl)-2,3,5-trimethylbenzoquinone

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

6-(6-Carboxy-1-phenylhexyl)-2,3,5-trimethylbenzoquinone (29 g) was suspended in ether (500 ml). Diazomethane/ether solution was added until the raw material was disappeared on thin-layer chromatography. Then the ether layer was washed with water, dried over anhydrous sodium sulfate and concentrated. The concentrate was subjected to short column chromatography using silica gel (500 ml) and eluted with hexane/dichloromethane (1:1) to obtain 6-(6-methoxycarbonyl-1-phenylhexyl)-2,3,5-trimethylbenzoquinone (25.5 g) as an orange oil. This oil was dissolved in ether (200 ml) and stirred at room temperature for 1.5 hours with a solution containing sodium hydrosulfite (52 g) in water (200 ml). The ether layer was separated and washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain 6-(6-methoxycarbonyl-1-phenylhexyl)-2,3,5-trimethylhydroquinone (25.5 g). Then this compound was dissolved in dichloromethane (35 ml), imidazole (9.37 g, 2 eq.) was added, tert-butyldiphenylsilyl chloride (28.36 g, 1.5 eq.) was added dropwise with stirring at room temperature and the mixture was allowed to react overnight. The deposited imidazole hydrochloride was filtered off, and the filtrate was concentrated. The concentrate was subjected to column chromatography on silica gel (800 ml) and eluted with dichloromethane/hexane (2:1) to obtain the desired compound as a pale yellow viscous oil (46 g).

後処理

  1. washThen the ether layer was washed with water
  2. dry with materialdried over anhydrous sodium sulfate
  3. concentrationconcentrated
  4. washeluted with hexane/dichloromethane (1:1)

出典と根拠

ORDレコード
ord-98a121f609e9427bb4aaa292bc976ea2
出典データセット
uspto-grants-1996_10
特許番号
US05563129

関連ノート

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