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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603654Generated: November 4, 2026

Benzyl Bromide → HCID 86754829, compound

https://huagongshe.com/reaction/1603654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 88477147HCID 88477147—
CatalystSilverHCID 23954—
SolventAcetonitrileHCID 6342—
ProductHCID 86754829HCID 8675482959.1%

Reaction Steps

A solution of the silver salt of p-methoxybenzyl 2-[(3S, 4R)-4-mercapto-3-bromo-2-oxoazetidin-1-yl]-3-methylbut-2-enoate (10 g, 20 mmol) in dry acetonitrile (100 ml) was treated with benzyl bromide (4 g, 24 mmol) and the resulting mixture refluxed for 30 mins. the reaction was cooled to room temperature, filtered, evaporated to dryness and the residue purified by flash chromatography using 1:1 ether:pentane as the eluting solvent. Evaporation of the appropriate fractions gave the product as a white solid (5.8 g, 59%), mp 70-72° C. 1H NMR δ (CDCl3)1.93 (3H, s, CH3), 2.23 (3H, s, CH3), 3.66 (1H, dd, J=2.9, 17.5 Hz, SCH2), 3.79 (3H, s, OCH3), 4.52 (1H, d, J=1.8 Hz, H3), 4.95 (1H, d, J=1.9 Hz, H4), 5.08 (2H, q, J=12.0 Hz, CO2CH2), 6.84-6.90 (2H, m, 2.6Ph--H), 7.13-7.31 (7H, m, 3,5Ph--H,Ph--H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990102
Source datasetuspto-grants-1999_11
ORD IDord-f15e3363a9bb40f1a0ae3a6cbb637892
Source noteuspto-grants-1999_11