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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491735Generated: October 26, 2026

Acetic Anhydride → 4-[5-(Acetyloxy)-7-bromo-1,3-benzoxazol-2-yl]-2-fluorophenyl acetate

https://huagongshe.com/reaction/491735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1,4-DioxaneHCID 31275—
Reactant7-Bromo-2-(3-fluoro-4-hydroxyphenyl)benzo[d]oxazol-5-olHCID 135457325—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product4-[5-(Acetyloxy)-7-bromo-1,3-benzoxazol-2-yl]-2-fluorophenyl acetateHCID 2190737156%

Reaction Steps

Acetic anhydride (1.0 mL, 9.95 mmol) was added into a cold (0° C.) solution of 7-bromo-2-(3-fluoro-4-hydroxyphenyl)-1,3-benzoxazol-5-ol (1.24 g, 3.8 mmol), N,N-dimethylpyridin-4-amine (1.1 g, 9.18 mmol) and 1,4-dioxane (13 mL). The reaction mixture was allowed to warm up to room temperature and stirred for 20 h. Water (50 mL) was added to the reaction mixture extracted with EtOAc and dried over MgSO4. Evaporation and crystallization from EtOAc/hexane gave an off-white solid (0.87 g, 56% yield); MS m/e 408 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531564B2
Source datasetuspto-grants-2009_05
ORD IDord-6463f1ec85ef428396c930b445ec4920
Source noteuspto-grants-2009_05