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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733277Generated: November 1, 2026

Methyl iodide → HCID 57135386, compound

https://huagongshe.com/reaction/1733277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 57104178HCID 57104178—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 57135386HCID 57135386—

Reaction Steps

A Grignard solution is prepared in the usual manner from 10.7 g of magnesium in 30 ml of absolute ether and 68.8 g of methyl iodide in 100 ml of absolute ether. To this solution are added dropwise at 20°-25° C. over a period of 15-20 minutes 56.1 g of p-tert.butyl-α,β-dimethyl-cinnamaldehyde. After cooling to room temperature, the mixture is cautiously poured on to 200 g of ice and 150 g of technical ammonium chloride in 500 ml of water are added. The organic phase is separated, washed with water and sodium bicarbonate solution, dried over sodium sulphate and concentrated. By distillation there is obtained pure 3-(p-tert.butyl-phenyl)-1,2,3-trimethyl-allyl alcohol of boiling point 143°-148° C./0.001 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241058
Source datasetuspto-grants-1980_12
ORD IDord-65e64067ff8c4ab3a13ce832af7b440c
Source noteuspto-grants-1980_12