HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660087Generated: October 30, 2026
Water → 6-(But-3-en-1-yl)-3-ethoxycyclohex-2-en-1-one
https://huagongshe.com/reaction/1660087
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | 3-Ethoxycyclohex-2-ene-1-one | HCID 79216 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(But-3-en-1-yl)-3-ethoxycyclohex-2-en-1-one | HCID 12788306 | 29% |
Reaction Steps
A solution of 25 g. (0.178 mole) of 3-ethoxy-2-cyclohexen-1-one in 25 ml. of tetrahydrofuran is added dropwise (30 min.) to a -78° C. solution of 0.196 mole of lithium diisopropylamide (from 27.4 ml., 0.196 mole, of diisopropylamine and 85 ml., 0.187 mole, of 2.2 M n-butyl lithium in hexane) in 125 ml. of tetrahydrofuran. The reaction is stirred 30 minutes longer and then 65 ml. (0.374 mole) of hexamethylphosphoramide is added followed by 38.9 ml. (0.383 mole) of 4-bromo-1-butene. The reaction is then allowed to warm to room temperature, stirred 1.5 hours and quenched by addition of 5 ml. (0.277 mole) of water. Most of the solvent is removed under reduced pressure and the residue diluted with one liter ice water and 500 ml. ether. The ether extract is washed with two 300 ml. portions of water, dried over magnesium sulfate and evaporated. Distillation of the crude oil yields 10.1 g. (29%) of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04306097 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-4e62add751a14e668fa78f130791357d |
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| Source note | uspto-grants-1981_12 |
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