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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681507Generated: November 4, 2026

Acetic Anhydride → 3-[1-(Acetamido)tridecyl]-5-trimethylsilylfuran

https://huagongshe.com/reaction/1681507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant3-(1-Aminotridecyl)-5-trimethylsilylfuranHCID 15037077—
SolventDichloromethaneHCID 6344—
Product3-[1-(Acetamido)tridecyl]-5-trimethylsilylfuranHCID 15037078—

Reaction Steps

Acetic anhydride (0.1 ml) was added to a solution of 3-(1-aminotridecyl)-5-trimethylsilylfuran (89.8 mg, 0.27 mmol) and triethylamine (0.1 ml) in dichloromethane (1 ml) at room temperature. Stirring was continued overnight (14 hours) while the cooling bath attained room temperature. The residue, after solvent removal, was purified by preparative TLC 20×20 cm, 1000u; developed with 60% ethyl ether/hexane). The title amide was obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05171863
Source datasetuspto-grants-1992_12
ORD IDord-173658220ba04466a51d2bcf9a8680d0
Source noteuspto-grants-1992_12