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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367861Generated: November 2, 2026

tert-BUTYL CHLORIDE → 2,2,5,5-Tetramethyl-3-hexanone

https://huagongshe.com/reaction/2367861

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-BUTYL CHLORIDEHCID 10486—
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178418310HCID 178418310—
SolventCarbon DioxideHCID 280—
SolventTetrahydrofuranHCID 8028—
Product2,2,5,5-Tetramethyl-3-hexanoneHCID 136670—

Reaction Steps

2-chloro-2-methylpropane (75 g, 0.8 mol) was slowly added to magnesium pellets (19.5 g, 0.8 mol) in 800 mL of THF to make the Grignard reagent, tBuMgCl. This was added slowly to a mixture of cuprous chloride (49.5 g, 0.50 mol) and tertbutylacetylchloride (67.25 g, 0.50 mol), cooled to −50° C. in dry ice. After addition, the mixture was allowed to warm up to room temperature overnight. Most of the THF was removed by decreased pressure, followed by the addition of 500 mL of hexanes and 200 mL of 2M HCl. This mixture was filtered to remove the solid byproducts. The aqueous layer was washed 3× with 100 mL of hexanes, the hexanes layer washed 3× with 200 mL of 2M HCl, 2× with 200 mL of NaHCO3/water, 1× with 200 mL of water, and finally 1× with 200 mL of NaCl/water. The product mixture was then dried for an hour in MgSO4, which was subsequently removed by filtration. The hexane was then removed by atmospheric distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703103B2
Source datasetuspto-grants-2014_04
ORD IDord-2aaf5dbcffbe42a3bdfad3bf20802b35
Source noteuspto-grants-2014_04