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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395664Generated: November 1, 2026

Allyl bromide → HCID 131711766, compound

https://huagongshe.com/reaction/1395664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 131711767HCID 131711767—
SolventMethanolHCID 887—
ProductHCID 131711766HCID 131711766—

Reaction Steps

533 Mg. (2 meq.) of H-Tyr-D-Ala-OMe in 80 ml. of methanol with 400 mg. (4 meq.) of powdered KHCl3 and 484 mg. (4 meq.) of allyl bromide were refluxed 2.5 hours under nitrogen. The solution was evaporated to dryness and dried in vacuo over KOH. The desired product was purified by high performance liquid chromatography using reverse phase C-18 column and eluting with 0.1 molar NH4OAc ph 4.2 containing 23% acetonitrile. The mass spectrometric analysis of the isolated product confirms the presence of an N-allyl group on the dipeptide. TLC (S. C., BAW peptidechlorine spray) indicated the presence of one major component RF 0.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04205069
Source datasetuspto-grants-1980_05
ORD IDord-1f072fe6dcd840c5af64c5e53999d1d1
Source noteuspto-grants-1980_05