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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629685Generated: October 31, 2026

Methanol → HCID 66774323, compound

https://huagongshe.com/reaction/1629685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 13406056HCID 13406056—
SolventPyridineHCID 1049—
ProductHCID 66774323HCID 66774323—

Reaction Steps

Compound 4 is O-Acetylated using well known literature procedures (Protective Groups in Organic Synthesis, 3rd edition, 1999, pp. 150-160 and references cited therein and in Greene, T. W. and Wuts, P. G. M., eds, Wiley-Interscience, New York.) Acetic anhydride (2 to 2.5 eq.) and triethylamine (4 eq.) is added to a solution of 4 (1 eq.) and N,N-dimethylaminopyridine (0.1 eq.) in anhydrous pyridine. After stirring at room temperature for 1 hour the mixture is treated with methanol to quench excess acetic anhydride and evaporated. The residue is redissolved in ethyl acetate, washed extensively with aqueous NaHCO3, dried over anhydrous Na2SO4, filtered, and evaporated. The compound is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791083B2
Source datasetuspto-grants-2014_07
ORD IDord-f8244bde9a57471e90d9084bb69e4799
Source noteuspto-grants-2014_07