HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486627Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 14695112, compound
https://huagongshe.com/reaction/486627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Calcium Hydroxide | HCID 6093208 | — |
| Reactant | HCID 14695111 | HCID 14695111 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14695112 | HCID 14695112 | 30.8% |
Reaction Steps
2-(4-Chlorobenzyl)-2,5,5-trimethyl-1-methylenecyclopentane (6.1 g) was dissolved in 60 ml of chloroform, followed by the addition of 8.5 g of m-chloroperbenzoic acid. The resultant mixture was stirred for 5 hours under ice cooling. Calcium hydroxide (4.0 g) was added, followed by stirring at room temperature for 30 minutes. A solid thus precipitated was filtered off. From the chloroform layer as the filtrate, chloroform was distilled off under reduced pressure to obtain a colorless oily substance. The substance was subjected to and purified by chromatography on a silica gel column (eluent: 6:1 mixed solvent of n-hexane and methylene chloride), thereby obtaining 2.0 g of 4-(4-chlorobenzyl)-4,7,7-trimethyl-1-oxaspiro[2.4]heptane used in the above Preparation Example.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292764 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-837d6bba712a4a5ea7a2ea01033808fc |
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| Source note | uspto-grants-1994_03 |
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