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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344627Generated: October 30, 2026

Formaldehyde → 3-Methyl-1-heptanol

https://huagongshe.com/reaction/344627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant1,2-DibromoethaneHCID 7839—
ReactantHCID 523771HCID 523771—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-1-heptanolHCID 517883—

Reaction Steps

Magnesium turnings (2.0 g, 82.3 mmol) are etched with iodine, and 1 ml of a solution of 96% 1-chloro-2-methylhexane (11 g, 78.5 mmol) in tetrahydrofuran (10 ml) is added at 60° C. The reaction is started by the addition of 1,2-dibromoethane (0.2 ml), then the rest of the solution of 1-chloro-2-methylhexane is added dropwise. After dilution with tetrahydrofuran (15 ml) the mixture is stirred under reflux for 2.5 h. Gaseous formaldehyde is passed through the solution, whose temperature is kept at from 40° C. to 50° C. The mixture is stirred for a further 1 h at room temperature, then 30% sulfuric acid (10 ml) is added to hydrolyze the Grignard compound. The mixture is steam distilled and the distillate is extracted several times with ether. The extract is washed with sodium chloride solution, dried over sodium sulfate, and evaporated down.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053223
Source datasetuspto-grants-1991_10
ORD IDord-e93962146ab94a6893b7a0123a0b8faf
Source noteuspto-grants-1991_10