HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968484Generated: October 28, 2026
Tosylmethyl isocyanide → HCID 69280233, compound
https://huagongshe.com/reaction/968484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 1-Benzyl-hexahydro-4H-azepin-4-one | HCID 1514350 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 69280233 | HCID 69280233 | 112% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304052B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-6da05282a77446aa948bc2b4fce5f471 |
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| Source note | uspto-grants-2007_12 |
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