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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280469Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonyl chloride

https://huagongshe.com/de/reaction/280469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfuric AcidHCID 1118—
EduktSulfur DioxideHCID 1119—
Edukt2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-amineHCID 91697—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelButyl ChlorideHCID 8005—
Produkt2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonyl chlorideHCID 13424179—

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

A diazonium salt was prepared by adding 13.8 g of sodium nitrite to a suspension of 32.6 g of 7-amino-2,3-dihydro-2,2-dimethylbenzofuran and 40 ml of concentrated sulfuric acid in 200 ml water cooled 0° to 5° C. After stirring for about 0.4 hour at 0° to 5° C., the diazonium salt suspension was poured in one portion into a mixture consisting of 170 ml of acetic acid, 40 ml of concentrated hydrochloric acid, 17 g of cupric chloride dihydrate and 30 ml of sulfur dioxide and cooled by 10° C. by an ice-water bath. The mixture was stirred about 1 hour at 15° to 25° C. Then 400 ml of 1-chlorobutane and 200 ml of water was added and the mixture was stirred and heated at 35° C. for 5 hours. After cooling to room temperature, the organic layer was separated, washed with saturated aqueous NaHCO3 and water, and dried over sodium sulfate for 0.5 hour. The solvent was evaporated under reduced pressure at less than 45° C. to give 26 g of crude 2,3-dihydro-2,2-dimethyl-7-benzofuransulfonyl chloride as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04589909
Quelldatensatzuspto-grants-1986_05
ORD IDord-60a3e52a31ba4a4f8cbe8a70a77473b0
Quellennotizuspto-grants-1986_05