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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393065Generated: October 30, 2026

Acetic Anhydride → HCID 131720814, compound

https://huagongshe.com/reaction/2393065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantBetulinHCID 72326—
SolventPyridineHCID 1049—
ProductHCID 131720814HCID 13172081487%

Reaction Steps

Then, the secondary hydroxyl group of monoprotected betulin compound 4 was acetylated using acetic anhydride in pyridine (Ac2O/pyridine), to yield monoprotected betulin acetate compound 5 of scheme 2 in 87% yield. Other acetylating agents also can be used. Examples of other acetylating agents include, but are not limited to, acetyl chloride; pentafluorophenyl acetate, triethylamine, and dimethylformamide; acetic anhydride, boron trifluoride etherate, and tetrahydrofuran; ketene, potassium tert-butoxide, and tetrahydrofuran; and acetic acid and trimethylsilyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05804575
Source datasetuspto-grants-1998_09
ORD IDord-aa279f192eda431db178ac2c07d6b0a9
Source noteuspto-grants-1998_09