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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646547Generated: October 31, 2026

Ozone → 2-(4-Chloro-2-indanyl) ethanol

https://huagongshe.com/reaction/1646547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantHCID 19801146HCID 19801146—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-(4-Chloro-2-indanyl) ethanolHCID 54363101—

Reaction Steps

Amalgamated zinc (prepared from zinc powder (6 g), mercuric chloride (0.6 g)) was heated under reflux for 7 hours with 2-allyl-4-chloro-indan-1-one (3 g), toluene (20 ml), conc. hydrochloric acid (20 ml), water (8 ml) and acetic acid (2 ml). Upon cooling conventional work-up gave a crude product which was purified by chromatography (silica/hexane) to give a 2-allyl-4-chloroindane (1.8 g). 2-Allyl-4-chloroindane (0.8 g) in dry methanol (10 ml) and dry dichloromethane (2 ml) was reacted at -35° with ozone until the blue colour persisted. After purging with nitrogen the solution was stirred 16 hours with dimethyl sulphide (2.58 g). The volatiles were removed and the residue taken up in tetrahydrofuran (10 ml) and heated under reflux with 4-toluenesulphonic acid (30 mg) and water (circa 0.5 ml) for 2 hours. After conventional work up the product, 2-(4-chloro-2-indanyl) ethanol, was obtained as a yellow oil (0.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180737
Source datasetuspto-grants-1993_01
ORD IDord-a2b0c7514c7e45569e60cd63199b343b
Source noteuspto-grants-1993_01