HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917596Generated: October 27, 2026
Pivaloyl chloride → Ethyl 2,2,7,7-tetramethyl-6-oxooct-4-ynoate
https://huagongshe.com/reaction/1917596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Ethyl 2,2-dimethylpent-4-ynoate | HCID 14459632 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 2,2,7,7-tetramethyl-6-oxooct-4-ynoate | HCID 58505758 | 54% |
Reaction Steps
To a solution of ethyl 2,2-dimethylpent-4-ynoate (1.00 g, 6.5 mmol), 2,2-dimethyl-propionyl chloride (0.8 mL, 6.5 mmol), and dichlorobis(triphenylphosphine) palladium(II) (460 mg, 0.65 mmol) in triethylamine (TEA) (12 mL) is added CuI (62 mg, 0.32 mmol). The mixture is stirred at 23° C. for 3 h then partitioned between Et2O and saturated aqueous NH4Cl. The organics are washed with water, dried with MgSO4, filtered, and concentrated in vacuo. The residue is purified by flash chromatography (SiO2, hexanes to 10% EtOAc in hexanes) to give the title intermediate (828 mg, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618300B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-aee81fe8b83f4ef4828c1e247b05dcf9 |
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| Source note | uspto-grants-2013_12 |
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