HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388860Generated: October 27, 2026
Tetrahydrofuran → 2,6-Dimethyl-5-methylene-1-hepten-4-ol
https://huagongshe.com/reaction/1388860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | 3-Methyl-2-methylenebutyraldehyde | HCID 78131 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Dimethyl-5-methylene-1-hepten-4-ol | HCID 20237380 | 73.8% |
Reaction Steps
A mixture of magnesium turnings (146 grams) and tetrahydrofuran (2,000 grams) is heated to reflux with vigorous agitation. To this mixture is added a mixture of 3-chloro-2-methylpropene (500 grams), toluene (75 grams), and 3-methyl-2-methylenebutanal (500 grams prepared according to Example I), at such a rate as to maintain reflux. The addition requires approximately four hours. The mass is stirred at reflux for 30 minutes and is then cooled to room temperature and quenched into excess ice cold 10% aqueous acetic acid mixture. The organic layer is washed successively with an equal volume of water, saturated sodium carbonate solution and saturated salt solution. Rapid distillation at 3-12 mm/Hg pressure using a short column followed by careful redistillation (after bulking) through a 12"×1" Goodloe packed column yields 580 grams of 2,6-dimethyl-5-methylene-1-hepten-4-ol, boiling point range 73°-78° C. at 9 mm/Hg pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04433695 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-da864d17f29a4d1aaefd55a61f3eb705 |
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| Source note | uspto-grants-1984_02 |
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