Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279358Generated: October 30, 2026

Tosylmethyl isocyanide → HCID 22624692, compound

https://huagongshe.com/reaction/279358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
ReactantHCID 15489190HCID 15489190—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22624692HCID 22624692—

Reaction Steps

To a −15° C. solution of 1 eq. of N-[2-[4-oxocyclohexyl]propyl] 2-propanesulfonamide (see Preparation 2) and 1 eq. of tosylmethyl isocyanide in dimethoxyethane is added a solution of 2.8 eq. of potassium t-butoxide in t-butanol. The cooling bath is removed and the mixture is stirred for three hours. The mixture is then diluted with water and extracted three times with diethyl ether. The combined organic extracts are dried over MgSO4, filtered and concentrated in vacuo to provide the crude material. Chromatography (silica gel) of the crude material affords the purified title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362230B1
Source datasetuspto-grants-2002_03
ORD IDord-ad3ec5c56b264f8da0c09ef773c6b855
Source noteuspto-grants-2002_03