Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant7-Phenyl-1H-indeneHCID 12942386—
SolventChloroformHCID 6212—
Product5-Phenyl-6,6a-dihydro-1aH-indeno[1,2-b]oxireneHCID 1327928097.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04346251
Source datasetuspto-grants-1982_08
ORD IDord-24ac44474ffa4354bba5e9fe639851f8
Source noteuspto-grants-1982_08