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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968484Generated: October 28, 2026

Tosylmethyl isocyanide → HCID 69280233, compound

https://huagongshe.com/reaction/968484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
Reactant1-Benzyl-hexahydro-4H-azepin-4-oneHCID 1514350—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solventtert-ButanolHCID 6386—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 69280233HCID 69280233112%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of hexahydro-1-(phenylmethyl)-4H-azepin-4-one (0.2 mol) and 4-toluene-sulfonylmethyl isocyanide (0.25 mol) in DMF (200 ml) was stirred at 0° C. A solution of potassium tert-butoxide (0.4 mol) in a mixture of 2-methyl-2-propanol (200 ml) and 1,2-dimethoxyethane (200 ml) was added dropwise at 0° C. The mixture was allowed to reach room temperature and stirring was continued for 1 hour. The mixture was stirred in water and this mixture was extracted with DCM. The separated organic layer was dried, filtered and the solvent was evaporated, yielding 48 g of (±)-hexahydro-1-(phenylmethyl)-1H-azepine-4-carbonitrile (intermediate 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304052B2
Source datasetuspto-grants-2007_12
ORD IDord-6da05282a77446aa948bc2b4fce5f471
Source noteuspto-grants-2007_12