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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864798Generated: October 31, 2026

Trityl chloride → 6-Bromo-3-trityl-3H-benzooxazol-2-one

https://huagongshe.com/reaction/1864798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant6-Bromo-2(3H)-benzoxazoloneHCID 29859—
SolventDichloromethaneHCID 6344—
Product6-Bromo-3-trityl-3H-benzooxazol-2-oneHCID 3097018—

Reaction Steps

To a solution of 6-bromo-3H-benzoxazol-2-one (15 g; ca. 0.07 mol, containing 8-9% 3H-benzooxazol-2-one) and triethylamine (11.1 mL, 0.08 mol) in DCM (250 mL) was added trityl chloride (21.5 g, 0.08 mol). The solution was stirred at room temperature for 18 h and was then washed with distilled water (3×250 mL), brine (250 mL) and dried (MgSO4), filtered and evaporated to give an off-white colored solid. The product was dissolved in refluxing EtOAc then allowed to cool to room temperature with constant stirring for several hours. The solids were collected (21.16 g) and the filtrate was concentrated until precipitation occurred, re-heated (reflux) for several hours and allowed to cool with stirring to encourage a second crystallization (7.88 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625889B2
Source datasetuspto-grants-2009_12
ORD IDord-803e9630e1164f829161b530594885da
Source noteuspto-grants-2009_12