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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876723Generated: October 30, 2026

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

https://huagongshe.com/reaction/876723

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 numberUS08987254B2
Source datasetuspto-grants-2015_03
ORD IDord-5f082fdf4aa8408b8482e07ac463f1f6
Source noteuspto-grants-2015_03