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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278330Generated: October 25, 2026

Acetic Anhydride → HCID 67958188, compound

https://huagongshe.com/reaction/2278330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-BromoresorcinolHCID 604810—
SolventDichloromethaneHCID 6344—
ProductHCID 67958188HCID 67958188—

Reaction Steps

To a solution of 2-bromo-1,3-benzenediol (3.028 g, 16.02 mmol) in dichloromethane (70 ml), TEA (3.35 ml, 24.03 mmol) and acetic anhydride (1.512 ml, 16.02 mmol) were added under stirring. The reaction mixture was stirred at room temperature overnight. The reaction was quenched with a saturated solution of ammonium chloride (100 ml), and extracted with ethyl acetate (3 times 70 ml). The combined organic layers were dried over sodium sulphate, filtered and evaporated to afford the title compound as a black oil which was used directly used in the next step. (3.028 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133175B2
Source datasetuspto-grants-2015_09
ORD IDord-454ce238aa5c4eaab62616817c55a9f2
Source noteuspto-grants-2015_09