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HRID 748673作成日:2026年10月26日

Hexane → HCID 59750776、化合物

https://huagongshe.com/reaction/748673

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物tert-Butyl(4-iodobutoxy)dimethylsilaneHCID 4250746—
反応物2-(((4-Chlorophenyl)sulfonyl)methyl)-1,4-difluorobenzeneHCID 9901028—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物HCID 59750776HCID 59750776—

反応条件

温度-78 °C

反応手順

In an argon gas stream and at −78° C., n-butyl lithium (a 1.57M hexane solution, 0.701 ml, 1.10 mmol) was added to a dimethoxyethane (5 ml) solution of the 2-[(4-chlorophenyl)sulfonylmethyl]-1,4-difluorobenzene (303 mg, 1.00 mmol) obtained in Example 5. The mixture was stirred at −78° C. for 1 hour and then, at room temperature for 30 minutes. The reaction mixture was cooled to −78° C., followed by the dropwise addition of 4-(t-butyldimethylsilyloxy)-1-iodobutane (0.260 ml, 1.00 mmol). While elevating the temperature of the reaction mixture to room temperature, stirring was conducted for 15 hours. Water was added to the reaction mixture, followed by extraction with diethyl ether. The extracts were combined, washed successively with water and brine, dried over MgSO4, and concentrated. The residue thus obtained was purified by medium-pressure chromatography on a silica gel column (8% ethyl acetate-hexane), whereby the title compound (401 mg, 82%) was obtained as a colorless solid. The resulting solid was recrystallized from hexane to yield colorless needle crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07399775B2
出典データセットuspto-grants-2008_07
ORD IDord-bce6c0c610834911a1353b39d816ba56
出典メモuspto-grants-2008_07