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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292246Generated: October 31, 2026

p-Bromobenzenesulfonyl chloride → HCID 54389295, compound

https://huagongshe.com/reaction/1292246

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantTriethylamineHCID 8471—
Reactanttert-butyl (2S)-2-amino-3-methylbutanoate hydrochlorideHCID 12490702—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 54389295HCID 54389295—

Reaction Steps

To a solution of 4-bromobenzenesulfonyl chloride (20 g, 0.070 mol) and (L)-valine-tert-butyl ester, hydrochloride (16.4 g, 0.078 mol) in aqueous tetrahydrofuran (400 mL, 1:1) was added dropwise triethylamine (15.6 g, 0.15 mol). The reaction mixture was stirred at room temperature for 16 hours, then diluted with aqueous HCl (1M, 300 mL) and ethyl acetate (300 mL). The layers were separated and the organic portion was washed with brine, dried (MgSO4), filtered, and the filtrate was concentrated in vacuo leaving a white solid. The crude product was recrystallized from hexane/ethyl acetate to give the title compound as white crystalline needles. Yield: 19.7 g (67%); mp 108°-110°;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756545
Source datasetuspto-grants-1998_05
ORD IDord-1c98207db52742b5a4c553743ee172ae
Source noteuspto-grants-1998_05