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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943855Generated: November 2, 2026

Hydrochloric Acid → Benzyl 2-chloro-6-fluoro-3-(propylsulfonamido)benzoate

https://huagongshe.com/reaction/1943855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactantbenzyl chloro-6-fluoro-3-(N-(propylsulfonyl)propylsulfonamido)benzoateHCID 58095368—
SolventLithium HydroxideHCID 3939—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 2-chloro-6-fluoro-3-(propylsulfonamido)benzoateHCID 6684081953.9%

Reaction Steps

Benzyl 2-chloro-6-fluoro-3-(N-(propylsulfonyl) propylsulfonamido)benzoate (413.2 mg, 0.840 mmol) was dissolved in THF (8.4 mL) and 2.0M aqueous LiOH (1.26 mL). The mixture was refluxed for 16 hours and then allowed to cool to ambient temperature. The mixture was acidified to a pH of 0 with 1.0M HCl (5.0 mL) and then adjusted to a pH of 4 using saturated sodium bicarbonate. The mixture was extracted with EtOAc (2×). The extracts were washed with water (2×) and brine (1×), dried over sodium sulfate and concentrated to afford benzyl 2-chloro-6-fluoro-3-(propylsulfonamido)benzoate (174.5 mg, 0.4523 mmol, 53.9% yield). MS (APCI-neg) m/z=384.1 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-735e2ba1a858430fa932fb93541aad5c
Source noteuspto-grants-2013_03