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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172163Generated: October 31, 2026

Boron tribromide → HCID 58156887, compound

https://huagongshe.com/reaction/2172163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 66616207HCID 66616207—
SolventDichloromethaneHCID 6344—
ProductHCID 58156887HCID 58156887100%

Reaction Steps

Methyl 4-[5-(4-isopropylphenyl)-2-oxo-1,3,4-thiadiazol-3(2H)-yl]benzoate (0.20 g, 0.56 mmol) in dichloromethane (10 mL) is then treated with boron tribromide (1M in dichloromethane, 1.7 mL, 1.7 mmol) at room temperature overnight. The volatiles are removed in vacuum and the residue is treated with water. The precipitate is collected and washed thoroughly with water to furnish the desired product, 4-[5-(4-isopropylphenyl)-2-oxo-1,3,4-thiadiazol-3(2H)-yl]benzoic acid (0.19 g, 100%), m.p. 205-208° C. 1H NMR (CDCl3, 300 MHz) δ (ppm) 1.30 (d, 6H) 2.92-3.06 (m, 1H), 7.35 (d, 2H), 7.70 (d, 2H), 8.11-8.23 (m, 4H). (ES+) m/z: 341.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051342B2
Source datasetuspto-grants-2015_06
ORD IDord-27290549fb0f42888869a7453f6ccc84
Source noteuspto-grants-2015_06