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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187303Generated: October 27, 2026

Hydrochloric Acid → HCID 58317006, compound

https://huagongshe.com/reaction/1187303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantLithium aluminum hydrideHCID 28112—
Reactant3-(2,5-Difluoro-benzenesulfonylamino)-2-fluoro-benzoic acid methyl esterHCID 58316996—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58317006HCID 5831700698.5%

Reaction Steps

To 3-(2,5-difluoro-benzenesulfonylamino)-2-fluoro-benzoic acid methyl ester (74, 0.955 g, 2.8 mmol) in 22 mL of tetrahydrofuran, lithium tetrahydroaluminate (6 mL, 1M in tetrahydrofuran, 6 mmol) is added at −40° C. under nitrogen. The reaction is allowed to warm to room temperature and stirred overnight. The reaction is poured into 1M aqueous sodium hydroxide, then neutralized with 1M aqueous hydrochloric acid. The solids are filtered through a bed of celite, and the celite bed is washed with ethyl acetate and tetrahydrofuran. The filtrate layers are separated and the aqueous layer is extracted with ethyl acetate. The organic layers are combined and washed with brine, dried over sodium sulfate, filtered and the filtrate is concentrated under vacuum. The resulting material is purified by silica gel column chromatography, eluting with ethyl acetate and dichloromethane. Appropriate fractions are combined and concentrated under vacuum to provide the desired compound (75, 0.875 g). MS (ESI) [M−H+]−=316.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673928B2
Source datasetuspto-grants-2014_03
ORD IDord-487fecff905d4b5aaf2d7b798fc26adb
Source noteuspto-grants-2014_03