HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67818Generated: October 30, 2026
Sodium Hydroxide → 5-Phenyl-6,6a-dihydro-1aH-indeno[1,2-b]oxirene
https://huagongshe.com/reaction/67818
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 7-Phenyl-1H-indene | HCID 12942386 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Phenyl-6,6a-dihydro-1aH-indeno[1,2-b]oxirene | HCID 13279280 | 97.9% |
Reaction Steps
A stirred solution of 47.5 g (0.234 mole) of m-chloroperbenzoic acid (85% purity) in 390 ml of chloroform was cooled to 0° C. To this was added dropwise a solution of 45 g (0.234 mole) of 7-phenyl-1H-indene (which may be prepared as in Example 1G) in 110 ml of chloroform. After complete addition, the mixture was stirred for 21/2 hours, then was allowed to stand for 21 hours at 0° C. With the temperature in the range of 0°-5° C., 100 ml of a 10% aqueous solution of sodium hydroxide, then 50 ml of a 10% aqueous solution of sodium sulfate, were added dropwise with stirring. After complete addition the two-phase mixture was stirred for 30 minutes. The organic phase was separated, washed first with a dilute aqueous solution of sodium bicarbonate, then with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to give 47.7 g of 1,2-epoxy-4-phenyindane as a pale yellow oil, 97% purity by gas chromatographic analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04346251 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-24ac44474ffa4354bba5e9fe639851f8 |
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| Source note | uspto-grants-1982_08 |
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