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HRID 703594作成日:2026年10月27日

Thioacetic acid → HCID 18642551、化合物

https://huagongshe.com/reaction/703594

反応式

関与物質

役割名称HCID仕込み量
反応物Thioacetic acidHCID 10484—
反応物Calcium HydroxideHCID 6093208—
反応物(2S,4R)-1-allyloxycarbonyl-2-(2-fluoroethyloxymethyl)-4-methylsulfonyloxypyrrolidineHCID 57165653—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物HCID 18642551HCID 18642551—

反応手順

To a solution of (2S,4R)-1-allyloxycarbonyl-2-(2-fluoroethyloxymethyl)-4-methanesulfonyloxypyrrolidine (17.30 g) and thioacetic S-acid (5.88 ml) in 4-methyl-2-pentanone (121 ml) was added calcium hydroxide (3.05 g) below 45° C. Solvent (40 ml) was removed under reduced pressure (50-60 mmHg), at 40°-45° C. The suspension was heated at 80°-85° C. for 5 hours. After cooling, water (30 ml) was added to the suspension. The insoluble material was filtered off and washed with ethyl acetate (50 ml). The filtrate and washing were collected. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (170 g) and eluted with a mixture of hexane and ethyl acetate (1:9-2:8) to give (2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(2-fluoroethyloxymethyl)pyrrolidine (13.80 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04983596
出典データセットuspto-grants-1991_01
ORD IDord-d916d6443ff341acad44e19cb037b4ff
出典メモuspto-grants-1991_01