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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941479Generated: November 2, 2026

Dimethyl Sulfide → HCID 21461371, compound

https://huagongshe.com/reaction/1941479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantBenzene, (diazomethyl)-HCID 136601—
ReactantBenzenesulfonamide, 4-methyl-N-[(4-nitrophenyl)methylene]-HCID 693818—
CatalystAcetic acid, rhodium(2+) saltHCID 21674—
SolventDichloromethaneHCID 6344—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 21461371HCID 21461371—

Reaction Steps

To a stirred solution of dimethylsulphide (5 μl, 0.07 mmol), rhodium (II) acetate (2 mg, 0.005 mmol) and N-(4-nitrobenzylidene)toluene-p-sulphonamide (102 mg, 0.33 mmol; J. C. S. Perkin I (1981) 2435-2442) in dichloromethane (2 ml) was added phenyldiazomethane (prepared as in Example 36; 8.11 ml of a 0.074M solution in t-butylmethylether) over a period of 12 hours. Upon completion of the addition the solvent was removed in vacuo and the residue was chromatographed using silica gel elating with 15:85 ethyl acetate:petrol to give the title compound as a mixture of trans and cis isomers. Trans isomer (48 mg, 37%) δH (CDCl3) 8.10-8.19(2H,m), 7.53-7.64(4H,m), 6.95-7.41(7H,m), 4.27(1H,d,J=6 Hz), 4.16(1H,d,J=6 Hz), 2.36(3H,s)ppm. Cis isomer (9 mg; 7%) δH (CDCl3) 8.23-8.33(2H,m); 7.15-7.60(11H,m), 4.13(1H,d,J=2 Hz) 3.87(1H,d,J=2 Hz) 1.68(3H,s)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703246
Source datasetuspto-grants-1997_12
ORD IDord-3a546c5989554edaae12248e383e4923
Source noteuspto-grants-1997_12