Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488215Generated: October 30, 2026

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

https://huagongshe.com/reaction/488215

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 numberUS05298633
Source datasetuspto-grants-1994_03
ORD IDord-c22b1edad787426a833a06de04e35160
Source noteuspto-grants-1994_03