HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 68130736, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | HCID 131710446 | HCID 131710446 | — |
| Product | HCID 68130736 | HCID 68130736 | — |
Reaction Steps
A solution of benzhydryl 3-diazomethyl-7β-(2-thienylacetamido)-ceph-3-em-4-carboxylate (9.0 × 10-4 mole), prepared by the process described in Example 2, and ethanethiol (5 ml.) is stirred at room temperature for 15 minutes. The excess ethanethiol is removed in vacuo and the residue chromatographed over silica gel with chloroform:acetone (10:1) to give benzhydryl 3-ethylthiomethyl-7β-(2-thienylacetamido)-ceph-3-em-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03979384 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-9492f837debd4bf39c69bb956aeb82ef |
| Source note | uspto-grants-1976_09 |