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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381406Generated: November 1, 2026

Acetic Anhydride → HCID 66891631, compound

https://huagongshe.com/reaction/2381406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1-(5-Methyl-3-nitro-pyrazol-1-yl)-propan-2-olHCID 66875310—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66891631HCID 6689163175%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1-(5-Methyl-3-Nitro-Pyrazol-1-Yl)-Propan-2-ol (440 Mg, 2.5 Mmol) in methylene chloride at 25° C. was treated with triethylamine (1.1 mL, 7.7 mmol), catalytic dimethylaminopyridine and acetic anhydride (0.29 mL, 3.0 mmol). The reaction was stirred at 25° C. for 1.5 h. At this time, the reaction was poured into water and was extracted into methylene chloride. The organics were concentrated in vacuo to afford acetic acid 1-methyl-2-(5-methyl-3-nitro-pyrazol-1-yl)-ethyl ester (440 mg, 75%) as a white solid which was used without further purification; ES+-HRMS m/e calcd for C9H13N3O4 [M+Na+] 250.0798, found 250.0798.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258134B2
Source datasetuspto-grants-2012_09
ORD IDord-4467dd724d114afc86a5f80d5267035d
Source noteuspto-grants-2012_09