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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603655Generated: November 1, 2026

Oxygen → HCID 54383686, compound

https://huagongshe.com/reaction/1603655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantDimethyl SulfideHCID 1068—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86754829HCID 86754829—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 54383686HCID 5438368664.3%

Reaction Steps

Ozonised oxygen was bubbled through a solution of p-methoxybenzyl 2-[(3S, 4R)-4-benzylthio-3-bromo-2-oxoazetidin-1-yl]-3-methylbut-2-enoate (2 g, 4 mmol) in dichloromethane (40 ml) at -78° C. and the reaction monitored by infra-red spectroscopy. When the band at 1780 cm-1 had disappeared, methanol (4 ml) together with a trace of sodium methoxide and dimethyl sulfide (1 ml) was added and stirring continued at room temperature for 16 h. The reaction was evaporated 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 colourless oil (0.7 g, 64%). 1H NMR δ (CDCl3) 3.87 (2H, s, SCH2), 4.52 (1H, m, H4), 4.69 (1H, d, H3) 5.85 (1H, bs, NH), 7.18-7.39 (5H, m, Ph--H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990102
Source datasetuspto-grants-1999_11
ORD IDord-e853c40451bf4f3189242e114ed929e7
Source noteuspto-grants-1999_11