HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638789Generated: November 2, 2026
Ammonium Chloride → HCID 68576919, compound
https://huagongshe.com/reaction/638789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Reactant | 2-Cyclohexen-1-one, 2-methyl- | HCID 136887 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 68576919 | HCID 68576919 | — |
Reaction Steps
To a solution of LDA (prepared from BuLi, 1.6 M in hexane, 75 ml, 0.12 mol and diisopropylamine, 12.2 g, 0.12 mol) in THF (50 ml) was added 2-methyl-cyclohex-2-enone (11.0 g, 0.1 mol) at −78° C. The mixture was stirred for 1 h at −78° C. and prenyl bromide 17.88 g, 0.12 mol) was added. The mixture was stirred over night, while the temperature was allowed to rise to room temperature. MTBE (50 ml) and sat. NH4Cl were added, the organic phase was separated and washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was distilled in a Kugelrohr oven to yield 9.8 g (55%) of a slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691802B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-f587ac21a9c84c1588cbdfb73e3c670e |
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| Source note | uspto-grants-2010_04 |
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