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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646603Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 19801181, compound

https://huagongshe.com/reaction/1646603

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantChlorosuccinimideHCID 31398—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantHCID 19801182HCID 19801182—
Solvent1,2-DichloroethaneHCID 11—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 19801181HCID 1980118140.7%

Reaction Steps

8 g of 3-trimethylsilyloxy-7-(2-propenyl)-indene in 25 ml of 1,2-dichloroethane is cooled to 0° C.; 31 g of N-chlorosuccinimide in 80 ml of dichloroethane is introduced over 25 minutes, with agitation for 30 minutes at 0° C.; 0.6 g of N-chlorosuccinimide in 15 ml of dichloroethane and a few mg of paratoluene sulphonic acid are added. After 30 minutes of agitation at 0° C., the reaction mixture is poured over an iced aqueous solution saturated with monopotassium phosphate, with agitation for 16 hours at 20° C. After decanting and extracting with methylene chloride, the extracts are dried, and concentrated to dryness under reduced pressure. The residue is chromatographed on silica, eluting with a hexane-isopropyl ether mixture (7-3). The fractions recovered are concentrated and chromatographed again on silica, eluting with a hexane-isopropyl ether mixture (3-1) and 2.75 g of expected product is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180741
Source datasetuspto-grants-1993_01
ORD IDord-1c17a3994839450d86561c344de848fa
Source noteuspto-grants-1993_01