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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874245Generated: October 30, 2026

Phenethyl bromide → HCID 67071414, compound

https://huagongshe.com/reaction/874245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67071652HCID 67071652—
SolventDichloromethaneHCID 6344—
ProductHCID 67071414HCID 67071414—

Reaction Steps

A suspension of (E)-3-[4-oxo-spiro(chromane-2,3′-pyrrolidine)-6-yl]-acrylic acid methyl ester (500 mg, 1.55 mmol, Intermediate 1) in DCM (15 ml) was treated with DIPEA (0.33 ml, 1.86 mmol) and phenethyl bromide (0.251 ml, 1.86 mmol), and stirred at RT for 8 days. The mixture was concentrated and the crude residue was purified by column chromatography (eluent: petroleum ether/EtOAc 7:3) to give (±)-(E)-3-[1′-(2-phenyl-ethyl)-4-oxo-spiro(chromane-2,3′-pyrrolidine)-6-yl]-acrylic acid methyl ester a yellow solid (280 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980877B2
Source datasetuspto-grants-2015_03
ORD IDord-8a4b2177e5544a27965d30ed6921d760
Source noteuspto-grants-2015_03