Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109876Generated: October 31, 2026

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

https://huagongshe.com/reaction/1109876

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, 1000 u; 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 numberUS05322953
Source datasetuspto-grants-1994_06
ORD IDord-7514cd4f56d243018ee7b03b57ff8237
Source noteuspto-grants-1994_06