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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195467Generated: October 27, 2026

Propargyl bromide → 1-(3-Butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene

https://huagongshe.com/reaction/1195467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantMagnesiumHCID 5462224—
Reactant1-(Chloromethyl)-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 10878929—
CatalystSodium IodideHCID 5238—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzeneHCID 2160841796.3%

Reaction Steps

A solution of chloromethyltrimethylhydroquinone dimethyl ether (7.5 g; 32 mmol) in THF (20 ml) was treated dropwise at 0° with a freshly Prepared solution of a Grignard reagent Prepared from 1.9 g of magnesium shavings and 4.91 ml (65 mmol) of propargyl bromide. After the addition of solid sodium iodide (0.42 g) the mixture was warmed to room temperature and stirred overnight. Thereafter, the reaction mixture was diluted with ether and washed with 2N hydrochloric acid. The ethereal solution was deacidified with bicarbonate, dried and freed from solvent. Distillation (0.04 mbar; 140° C.) of the residue gave 7.16 g of 1-(3-butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene; melting point: 54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110955
Source datasetuspto-grants-1992_05
ORD IDord-a79de7c350f041f6a90a4184f9a6ada7
Source noteuspto-grants-1992_05