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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381074Generated: November 1, 2026

Bromide ion → HCID 54337042, compound

https://huagongshe.com/reaction/1381074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant2-Methyl-2-pentenalHCID 12177—
Reactant1-Bromo-2-methylbutaneHCID 25254—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductHCID 54337042HCID 5433704234.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

0.72 g (29.8 mg atoms) of magnesium in 3 ml of absolute ether are placed in an apparatus which is customary for Grignard reactions. While stirring there are subsequently added dropwise 5.0 g (33.1 mmol) of 1-bromo-2-methylbutane (90%) in 5 ml of absolute ether so that the ether boils constantly. After completing the addition of the bromide, the mixture is held at reflux temperature for a further 30 minutes, then cooled to 10° C. and a solution of 2.92 g (29.8 mmol) of 2-methyl-2-pentenal in 3 ml of absolute ether is added dropwise. The exothermic reaction causes the temperature to rise to 25° C. After refluxing for a further hour, the reaction product is worked-up with crushed ice and saturated ammonium chloride solution in the customary manner. After separating the aqueous phase, the organic layer is washed with saturated sodium chloride solution, subsequently dried and freed from solvent. The crude product (4.8 g) is distilled and yields 1.74 g of pure 3,6-dimethyl-6-nonen-5-ol (boiling point about 120° C./12 mm Hg; nD20 =1.4560), which has the following spectral data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585662
Source datasetuspto-grants-1986_04
ORD IDord-79f806fe2e874606b1bc46e8a8ad1f1f
Source noteuspto-grants-1986_04