Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Diethyl (1R,2R)-cyclohex-4-ene-1,2-dicarboxylate | HCID 12358152 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 13149-04-7 | HCID 11051760 | 127.3% |
Reaction Steps
A solution of 25 g of trans-4-cyclohexene-1,2-dicarboxylic acid diethyl ester in 140 ml of tetrahydrofuran is instilled in a suspension of 10 g of lithium aluminum hydride in 140 ml of tetrahydrofuran at room temperature and the mixture is then stirred for 3 hours at reflux temperature. It is cooled to 0° C., a mixture of tetrahydrofuran/water (1+1) is instilled slowly, stirred for 30 minutes, mixed with 150 ml of chloroform, filtered and the filtrate is concentrated by evaporation in a vacuum. The residue is distilled at 0.2 mm/Hg and at 150° C. in a bulb tube. In this way, 20 g of trans-1,6-dihydroxymethyl-3-cyclohexene is obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05187286 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-fe329a9fd14842c0b7192036058f5c2d |
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| Source note | uspto-grants-1993_02 |
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