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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608063Generated: October 31, 2026

Hydrochloric Acid → HCID 19855485, compound

https://huagongshe.com/reaction/1608063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14014982HCID 14014982—
ProductHCID 19855485HCID 19855485—

Reaction Steps

10 mmol of 6-amino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetic acid and 20 mmol of benzenesulphonyl chloride are warmed at 80° C. in 40 ml of 10% strength NaOH for 2 hours. The mixture is then acidified with concentrated HCl and the milky suspension is extracted by shaking twice with ethyl acetate. The combined ethyl acetate phases are rapidly extracted by shaking with 10% strength NaOH (product precipitates out of the ethyl acetate), the NaOH phase is acidified with concentrated HCl and extracted by shaking twice with ethyl acetate and the extract is dried over Na2SO4 and evaporated. The residue is boiled up in ethyl acetate and the mixture is filtered. The product crystallizes out after 2-3 hours in a refrigerator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868331
Source datasetuspto-grants-1989_09
ORD IDord-d6852a01d7d64d30be532251d84b096c
Source noteuspto-grants-1989_09