HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → HCID 11086987, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | n-(4-nitrobenzyl)benzamide | HCID 282107 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 11086987 | HCID 11086987 | 85% |
Reaction Steps
A solution of 3.7 mmol of N-(p-nitrobenzyl)-benzamide in thionyl chloride was refluxed under an inert atmosphere for 30 minutes and after cooling, the excess thionyl chloride was removed under vacuum to leave a solid residue. The residue was crystallized from dry cyclohexane under dry nitrogen (Note: the subsequent filtration had to be done under dry nitrogen also to obtain an 85% yield of the purified imidoyl--chloride melting at 71° to 73° C. (Lit. m.pt. 73--4 Huisgen et al--Loc. cit) which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059596 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-09e432bad7e34f9a93b89b58e18035dc |
| Source note | uspto-grants-1991_10 |