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HRID 414684作成日:2026年10月26日

Chlorosulfonic acid → 7-Hydroxy-6-chlorosulfonyl-4-methyl-1-indanone

https://huagongshe.com/reaction/414684

反応式

関与物質

役割名称HCID仕込み量
反応物Chlorosulfonic acidHCID 24638—
反応物7-Hydroxy-4-methyl-1-indanoneHCID 12436244—
溶媒Carbon TetrachlorideHCID 5943—
生成物7-Hydroxy-6-chlorosulfonyl-4-methyl-1-indanoneHCID 21281606—

反応手順

Into a solution of 90 ml of chlorosulfonic acid in 150 ml of carbon tetrachloride was added 30 g of 7-hydroxy-4-methyl-1-indanone gradually under an ice-cooling condition. The carbon tetrachloride layer was removed by separation, and one liter of ice-water was added into the residual layer then the mixture was stirred vigorously. The solid matter precipitated was collected by filtration, then washed with water to obtain 8.7 g of 7-hydroxy-6-chlorosulfonyl-4-methyl-1-indanone. This product was added, without purified, to a solution consisting of 31.4 g of stannous chloride dihydrate and 100 ml of concentrated hydrochloric acid, and the mixture was stirred at a room temperature for 4 hours. The reaction mixture was poured into 500 ml of ice-water, the crystals precipitated were collected by filtration, washed with water, dried to obtain 7.86 g of 7-hydroxy-6-mercapto-4-methyl-1-indanone. Next, this product was suspended, without purified, in 100 ml of methanol, then to this suspension was added 3.9 ml of methyl iodide and a solution of 5.1 g of sodium bicarbonate in 20 ml of water, the whole mixture was stirred at a room temperature for 1 hour. The mixture was concentrated under a reduced pressure to remove the solvent to dryness. The residue was purified by means of a silica gel column chromatography (eluent: chloroform) and recrystallized from ethanol to obtain 1.52 g of 7-hydroxy-4-methyl-6-methylthio-1-indanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04792628
出典データセットuspto-grants-1988_12
ORD IDord-ee4378ed482f4225aec302670aa1be6d
出典メモuspto-grants-1988_12