HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tosylmethyl isocyanide → 1,7,7-Trimethyl-bicyclo[2.2.1]heptane-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | HCID 9543187 | HCID 9543187 | — |
| Product | 1,7,7-Trimethyl-bicyclo[2.2.1]heptane-2-carbonitrile | HCID 18405550 | — |
Reaction Steps
(1R)-(+)-Camphor was converted to the nitrile using tosylmethyl isocyanide according to the procedure of O. H. Oldenziel (O. H. Oldenziel, D. van Leusen, and A. M. van Leusen J.Org.Chem. 1977, 42, 3114).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479531B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-ab03afc53d47427c8a72abb2a6f741a2 |
| Source note | uspto-grants-2002_11 |