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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660813Generated: October 28, 2026

Boron tribromide → HCID 57777311, compound

https://huagongshe.com/reaction/660813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 68838679HCID 68838679—
SolventDichloromethaneHCID 6344—
ProductHCID 57777311HCID 57777311—

Reaction Steps

To a solution of 5-(4-benzenesulfonyl-2-benzyloxyphenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one potassium in CH2Cl2 (5 mL), cooled in an ice/salt bath, is added dropwise BBr3 (4.8 mL, 1M in CH2Cl2). The mixture is stirred for 30 min then is quenched with water, basified with potassium carbonate, and separated. The aqueous layer is washed with ether, then lyophilized, and purified by preparative HPLC to afford the title compound as an amorphous solid: mp=126-180° C.; 1H NMR (DMSO-d6) δ 10.89 (br s, 1H), 7.93 (d, J=7.0 Hz, 2H), 7.66 (m, 4H), 7.42 (m, 2H), 4.56 (s, 2H); (M−1)−=367.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-8d8d27bac62441d0963a1a1f638a1c70
Source noteuspto-grants-2011_12