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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566857Generated: November 2, 2026

Allyl bromide → HCID 57242164, compound

https://huagongshe.com/reaction/566857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,2,4-Trimethyl-1-cyclohexanecarbaldehydeHCID 21263740—
SolventDiethyl EtherHCID 3283—
ProductHCID 57242164HCID 5724216480.8%

Reaction Steps

2,2,4-Trimethyl-1-cyclohexanecarbaldehyde (11 g, 72 mmole) in ether (100 ml) was added dropwise with stirring to a Grignard compound prepared from Mg (2.3 g) and allylbromide (10 g) in ether and refluxed for 2 h. After cooling, the mixture was hydrolyzed with NH4Cl-solution, then distilled at a bath temperature of 150°/0.5 hPa, to obtain 11.3 g (80%) of the desired product as a 2:1 mixture of 2 isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177400B1
Source datasetuspto-grants-2001_01
ORD IDord-f0f38d8eae4f4a478dc83ed23c8fc1bf
Source noteuspto-grants-2001_01