HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082191Generated: October 30, 2026
Chloroform → cis-1,2-Dihydroxymethylcyclohex-4-ene
https://huagongshe.com/reaction/2082191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Tetrahydrophthalic anhydride, cis- | HCID 98495 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | cis-1,2-Dihydroxymethylcyclohex-4-ene | HCID 11275057 | 89.9% |
Reaction Steps
A solution of 25 g of cis-4-cyclohexene-1,2-dicarboxylic acid anhydride 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/Torr and 150° C. on a bulb tube. After recrystallization of the distillate from toluene/pentane, 21 g of cis-1,6-dihydroxymethyl-3-cyclohexene is obtained as colorless crystals, melting point 33°-35° C.
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-1d094435d749402ca67fb1891241d8e7 |
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| Source note | uspto-grants-1993_02 |
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