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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534340Generated: October 31, 2026

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

https://huagongshe.com/reaction/1534340

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, 1000μ; 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 numberUS05089485
Source datasetuspto-grants-1992_02
ORD IDord-18e37563963d4170a4442945e62febe9
Source noteuspto-grants-1992_02