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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703830Generated: October 31, 2026

Dimethyl Sulfate → HCID 12557677, compound

https://huagongshe.com/reaction/1703830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12557675HCID 12557675—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 12557677HCID 12557677—

Reaction Steps

A mixture of 2-hydroxy-3-[N-[(4-methylphenyl)sulfonyl]-amino]-2,4,6-cycloheptatrien-1-one (14.5 g), potassium carbonate (12.5 g), dimethyl sulfate (12.5 g) and 2-butanone (145 ml) is heated at reflux for one hour. The mixture is filtered and the precipitate is washed with water and suspended in ethyl acetate. Hydrochloric acid (10%) is added until the solution is acidic. The organic phase is collected and dried over sodium sulfate. Evaporation of the solvent and crystallization of the residue from ethyl acetate-hexane gives 2-methoxy-7-[N-[(4-methylphenyl)-sulfonyl]amino]-2,4,6-cycloheptatrien-1-one, mp 163°-164° C. The above filtrate is evaporated and the residue is subjected to chromatography on silica gel using ethyl acetate-hexane (3:1). Evaporation of the eluates are crystallization of the residue from ethyl acetate gives 2-methoxy-3-[N-[(4-methylphenyl)sulfonyl]-N-methylamino]-2,4,6-cycloheptatrien-1-one, mp 101°-102° C and 2-methoxy-7-[N-[(4-methylphenyl)-sulfonyl]-N-methylmino]-2,4,6-cycloheptatrien-1-one, mp 94.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125625
Source datasetuspto-grants-1978_11
ORD IDord-c01a939d97844fa7b1ee1333e94a4e2f
Source noteuspto-grants-1978_11