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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374970Generated: October 27, 2026

Isoamylamine → n[3(s)-Benzyloxycarbonylamino-2(r)-hydroxy-4-phenylbutyl]n-isoamylamine

https://huagongshe.com/reaction/374970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamylamineHCID 7894—
Reactant(2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutaneHCID 9861019—
SolventIsopropanolHCID 3776—
Productn[3(s)-Benzyloxycarbonylamino-2(r)-hydroxy-4-phenylbutyl]n-isoamylamineHCID 1043012481%

Reaction Steps

A solution of N-benzyloxycarbonyl 3 (S)-amino-1,2-(S)-epoxy-4-phenylbutane (30.1 g, 0.10 mol) and 165mL of isoamylamine in 150 mL of isopropyl alcohol was heated to reflux for 2.5 hours. The solution was cooled to room temperature, concentrated in vacuo and then recrystallized. The product was isolated by filtration and from ethyl acetate/hexane to afford 31.7 g (81%) of N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482947
Source datasetuspto-grants-1996_01
ORD IDord-3c7112c140fd452e977e1d60b3165b4b
Source noteuspto-grants-1996_01