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HRID 747492作成日:2026年10月25日

Thiosulfuric acid, disodium salt, monohydrate → 1'-t-Butoxycarbonylspiro[benzo[c]thiophene-1-(3H),4'-piperidine]-2-oxide

https://huagongshe.com/reaction/747492

反応式

関与物質

役割名称HCID仕込み量
反応物Thiosulfuric acid, disodium salt, monohydrateHCID 108762—
反応物HCID 10566517HCID 10566517—
反応物Potassium hydroxy sulfiteHCID 23707502—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1'-t-Butoxycarbonylspiro[benzo[c]thiophene-1-(3H),4'-piperidine]-2-oxideHCID 10734560133.9%

反応条件

温度2.5 °C

反応手順

10.0 g of the crude tert-butyl spiro[benzo[c]thiophene-1(3H),4′-piperidine]-1′-carboxylate, obtained in Example 1, were added to 50 ml of methylene chloride and 150 ml of acetone followed by cooling to 0 to 5° C. A solution of 15.0 g (24.4 mmol) of Oxone™ in 75 ml of water was dropped in at 5° C. or lower followed by stirring for 3 hours at 0 to 5° C. A solution of 1.72 g (9.8 mmol) of sodium thiosulfate-hydrate in 50 ml of water was added followed by stirring for 30 minutes at 20 to 25° C. 100 ml of methylene chloride and 100 ml of water were then added followed by separation of the aqueous layer. After washing the organic layer with 100 ml of water, it was dried with anhydrous magnesium sulfate followed by distilling off the solvent to obtain 10.5 g of tert-butyl spiro[benzo[c]thiophene-1-(3H),4′-piperidine]-1′-carboxylate 2-oxide as a white foamy substance (crude yield: 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07396930B2
出典データセットuspto-grants-2008_07
ORD IDord-ce8b6c2d5796476bb29c33727972adc0
出典メモuspto-grants-2008_07