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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848799Generated: October 30, 2026

Toluene → HCID 54220385, compound

https://huagongshe.com/reaction/848799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantHCID 53647688HCID 53647688—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 54220385HCID 54220385—

Reaction Steps

A 22.4 g (0.067 mole) sample of the 1-bromo-3,3-bis(bromomethyl)-2-azetidinone was dissolved in 450 ml carbon tetrachloride. The insoluble residue (2.0 g) was discarded. A 7 ml (6.07 g, 0.067 mole) portion of toluene was added to the stirred solution. The reaction mixture was irradiated by a 275 watt General Electric Sunlamp and allowed to reflux for one hour. The reaction mixture was decanted hot from a small amount of residue on the stirrer and flask wall and then cooled in ice. White crystals were collected on a filter and dried in vacuo to yield 12.1 g of product. Mother liquor with a few seed crystals was kept cold overnight to yield a second crop of 1.0 g. Total yield of 13.1 g of 76.6% of 3,3-bis(bromomethyl)-2-azetidinone was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297475
Source datasetuspto-grants-1981_10
ORD IDord-48f914cba45d4f518d80d8b24a066cd7
Source noteuspto-grants-1981_10