HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898124Generated: October 30, 2026
Hexane → 1-Cyclopropyl-4,4-diethoxy-2-butyn-1-one
https://huagongshe.com/reaction/898124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 3,3-Diethoxypropyne | HCID 66285 | — |
| Reactant | N-Methoxy-N-methylcyclopropanecarboxamide | HCID 15643267 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Cyclopropyl-4,4-diethoxy-2-butyn-1-one | HCID 69293284 | 43.7% |
Reaction Steps
3,3-Diethoxy-1-propyne (10 mL, 70 mmol) was dissolved under argon in THF (150 mL) and cooled to −70° C. Then a 1.6 M solution of n-butyllithium in hexane (48 mL, 77 mmol) was added slowly at −70° C., then allowed to warm to −30° C. and stirred at −30° C. for 30 min, then cooled again to −70° C. Cyclopropanecarboxylic acid methoxy-methyl-amide (10 g, 77 mmol) was added at once at −70° C. (the temperature rose to −50°) then stirred without cooling until 0° C. was reached, then quenched with sat. NH4Cl solution (20 mL). Extraction: 2×AcOEt, 1× sat. NH4Cl, 1× sat. NaCl. The crude brown oil (15 g) was purified by chromatography on silica gel in heptane/ethyl acetate 10:1. One obtained 6 g (43%) of a yellowish oil. MS: m/z=151(M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351700B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-6e8c1b76083b43a18ceff5e97262da14 |
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| Source note | uspto-grants-2008_04 |
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