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HRID 432235作成日:2026年10月26日

Methanesulfonyl chloride → HCID 178505328、化合物

https://huagongshe.com/reaction/432235

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物HCID 178521634HCID 178521634—
溶媒PyridineHCID 1049—
生成物HCID 178505328HCID 17850532880.2%

反応手順

A solution of cis 3-((benzyloxy)methyl)-1-cyclobutanol (2.50 g, 0.0130 mol) in pyridine (50 mL) was cooled to 0° C. Methanesulfonyl chloride (1.21 mL, 1.79 g, 0.0126 mol) was added dropwise, keeping the temperature below 2° C. The mixture was stirred for four hours, and then poured into ice water (100 mL) and extracted with ethyl ether (2×50 mL). The combined organic layers were washed with water (3×50 mL) and brine (50 mL). The organic layer was dried over magnesium sulfate and the solvent was removed in vacuo to give cis 3-[(benzyloxy)methyl]cyclobutyl methanesulfonate (2.73 g, 0.0101 mol) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660744B1
出典データセットuspto-grants-2003_12
ORD IDord-91c9504295d64c2281d150cf9ea34aaa
出典メモuspto-grants-2003_12