HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847443Generated: October 30, 2026
Water → 1-(4-Chlorobenzyl)-1,2-epoxy-3,3-dimethyl-2-hydroxymethylcyclopentane
https://huagongshe.com/reaction/847443
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14721902 | HCID 14721902 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Chlorobenzyl)-1,2-epoxy-3,3-dimethyl-2-hydroxymethylcyclopentane | HCID 19020739 | 99.1% |
Reaction Steps
10.7 g (36.3 mmols) 1-(4-chlorobenzyl)-1,2-epoxy-3,3-dimethyl-2-methoxycarbonylcyclopentane prepared as described in (g) were dissolved in diethyl ether and the resulting solution was then added to a slurry of 1.5 g (36.6 mmols) lithium aluminium hydride in 50 ml diethyl ether at a rate such that reflux of the reaction mixture was maintained. Heating was continued for 5 minutes after the last addition of 1-(4-chlorobenzyl)-1,2-epoxy-3,3-dimethyl-2 -methoxycarbonylcyclopentane solution. 1.25 ml water were then added, followed by 1.25 ml 15% aqueous sodium hydroxide solution and a further 4 ml water. The solid was filtered off and the filtrate was then dried over anhydrous magnesium sulphate and flashed to give a clear oil which crystallised on cooling to give 9.6 g 1-(4-chlorobenzyl)-1,2-epoxy-3,3-dimethyl-2-hydroxymethylcyclopentane as a solid. m.pt. 36°-38° C., which can be reduced to 1-(4-chlorobenzyl)-3,3-dimethyl-2-hydroxy-2-hydroxymethylcyclopentane in a conventional method.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05142061 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-2921a209b67c4970b9ffdfd1205656f3 |
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| Source note | uspto-grants-1992_08 |
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