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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77572Generated: October 29, 2026

Ethyl Acetate → [1-Allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol

https://huagongshe.com/reaction/77572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant5-allyl-6a-(3-bromophenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazoleHCID 86762755—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product[1-Allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanolHCID 86762754101.8%

Reaction Steps

A 22° C. solution of 5-allyl-6a-(3-bromophenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazole (40 g, 129.4 mmol) in acetic acid (400 mL) is treated with zinc dust (42.3 g, 646.8 mmol) in one portion. The reaction is stirred vigorously at room temperature for 1 hour. Ethyl acetate (400 mL) is added and the mixture is filtered through diatomaceous earth. The filtrate is evaporated and the residue dried under vacuum. The residue is partitioned in water (300 mL) and MTBE (300 mL). The pH is adjusted to 8 with sodium hydroxide 50% w/w and the organic layer is separated, dried over sodium sulfate, and filtered. The filtrate is evaporated and the residue dried under vacuum to give the title compound (41 g, 97%). ES/MS (m/e): 311 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841293B1
Source datasetuspto-grants-2014_09
ORD IDord-9bb1bda83ed148a28080153061a92141
Source noteuspto-grants-2014_09