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HRID 222524作成日:2026年10月27日

Hydrochloric Acid → N-(2-Hydroxyethyl)-4-methoxy-N,2,6-trimethylbenzenesulfonamide

https://huagongshe.com/reaction/222524

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物WaterHCID 962—
反応物Sodium ChlorideHCID 5234—
反応物Chlorosulfonic acidHCID 24638—
反応物3,5-DimethylanisoleHCID 70126—
反応物N-MethylaminoethanolHCID 5247031—
溶媒DichloromethaneHCID 6344—
生成物N-(2-Hydroxyethyl)-4-methoxy-N,2,6-trimethylbenzenesulfonamideHCID 51712110—

反応条件

温度-7 °C

反応手順

10.00 kg (73.42 mol) of 3,5-dimethylanisol (A) were dissolved in 35.0 L of dichloromethane. After cooling to −15±5° C. a solution of 17.46 kg (149.86 mol) of chlorosulphonic acid in 20.0 L dichloromethane was metered in and the mixture was stirred for approx. another 30 minutes at −15±5° C. Then the reaction mixture was metered into a solution of 15.0 kg sodium chloride in 85.0 L of water that had been cooled to −7±5° C., and diluted with 15.0 L of dichloromethane. The organic phase was separated off, diluted with 15.0 L of dichloromethane and washed with 30.0 L of sodium hydrogen carbonate solution (5%). After separation of the organic phase once again and dilution with 10 L of dichloromethane, a solution of 11.58 kg (154.20 mol) N-methylaminoethanol in 10.0 L of dichloromethane was slowly metered in at 10±5° C. After the reaction had ended 45.0 L of HCl (3%) and 5.0 L of water were added. The organic phase was separated off, diluted with 10.0 L dichloromethane and the solvent was totally eliminated from the product (C) in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207335B2
出典データセットuspto-grants-2012_06
ORD IDord-9f1f5c869ec84a169535a776eb208804
出典メモuspto-grants-2012_06