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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | 3,3-Dimethylbutanoyl chloride | HCID 81514 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178418310 | HCID 178418310 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2,5,5-Tetramethyl-3-hexanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703103B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2aaf5dbcffbe42a3bdfad3bf20802b35 |
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| Source note | uspto-grants-2014_04 |
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