Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680283Generated: October 30, 2026

Dimethyl Sulfide → HCID 54570347, compound

https://huagongshe.com/reaction/1680283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 54051185HCID 54051185—
SolventTolueneHCID 1140—
ProductHCID 54570347HCID 54570347—

Reaction Steps

With stirring, 6 ml of dimethyl sulphide are added at 0° C. in an atmosphere of nitrogen to a suspension of 8.05 g of N-chlorosuccinimide in 200 ml of absolute toluene and then at -25° C. a solution of 12 g of crude 5-hydroxymethylphenyl-6-methoxy-indane-1-carboxylic acid methyl ester in 50 ml of absolute toluene is added. Upon completion of the addition, the mixture is further stirred for 90 minutes at -25° C. Then 8.3 ml of triethylamine are added to the reaction solution, which is stirred for a further 5 minutes and partitioned between 2×100 ml of 2 normal hydrochloric acid and 2×100 ml of ether. The organic phases are washed neutral, dried over sodium sulphate and evaporated to dryness in vacuo. The residue is chromatographed on silica gel with methylene chloride as eluant to yield 5-benzoyl-6-methoxy-indane-1-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04272547
Source datasetuspto-grants-1981_06
ORD IDord-b4142965ae004e629a2a34e446498b1a
Source noteuspto-grants-1981_06