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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090895Generated: October 31, 2026

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

https://huagongshe.com/reaction/1090895

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 amid was obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082954
Source datasetuspto-grants-1992_01
ORD IDord-a6687f0f2b054e17a62fab25756fb28a
Source noteuspto-grants-1992_01