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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389660Generated: October 30, 2026

Triethylamine → 1-[4-(16-Bromohexadecylamino)benzoyl]pyrrolidine

https://huagongshe.com/reaction/1389660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyrrolidineHCID 31268—
ReactantN-Carbobenzyloxy-4-(16-bromohexadecylamino)benzoyl chlorideHCID 20482544—
SolventDiethyl EtherHCID 3283—
Product1-[4-(16-Bromohexadecylamino)benzoyl]pyrrolidineHCID 13025412—

Reaction Steps

A solution of 6.0 g. of 4-[N-carbobenzyloxy-N-(16-bromohexadecyl)amino]benzoyl chloride and 1.2 g. triethylamine in 100 ml. warm ether is treated with 1.1 g. of pyrrolidine. After 1 hour at reflux, the precipitate is filtered off and washed with warm ether. After evaporation in dryness, the intermediate is dissolved in 50 ml. 30% hydrobromic/acetic acid and warmed at 50° for 2 hours. The solvents are evaporated and the product is partitioned between methylene chloride and water. The layers are separated and the methylene chloride is evaporated. The residue is crystallized from acetone to yield colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04245097
Source datasetuspto-grants-1981_01
ORD IDord-9466b6e6f08b44609e95bfe86ad3c4a5
Source noteuspto-grants-1981_01