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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376611Generated: November 2, 2026

Acetic Anhydride → HCID 22916681, compound

https://huagongshe.com/reaction/1376611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15428311HCID 15428311—
SolventDichloromethaneHCID 6344—
ProductHCID 22916681HCID 2291668195%

Reaction Steps

0.15 g of the 3-hydroxymethylimidazo[5,1-b]thiazole prepared in Preparation 55 was dissolved in 4 ml of dichloromethane, and the solution was stirred. To this was added 0.1 ml of acetic anhydride, and the mixture was stirred at room temperature for 3 hours. To the reaction solution was added 5 ml of a saturated aqueous solution of sodium hydrogencarbonate, and the organic layer was separated. The aqueous layer was extracted with dichloromethane (5 ml×2). The combined organic layers were dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure to give 0.181 g (yield 95%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663162
Source datasetuspto-grants-1997_09
ORD IDord-0f70cdc3e5954167b9031c7169948e14
Source noteuspto-grants-1997_09