HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → HCID 3890459, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 3890459 | HCID 3890459 | 95.2% |
Reaction Steps
To diazomethane (40 mmol) in ether (100 ml) at 0° C. was added phenylacetyl chloride (2.65 ml, 20 mmol). After 30 min at 0° C. the excess diazomethane and the ether were blown off with nitrogen, and then under vacuum to leave 1-diazo-3-phenyl-2-propanone as a yellow oil (3.05 g, 95%); δH (CDCl3) 7.2 (5H, S, aryl), 5.1 (1H, S, CH=N2), 3.5 (2H, S, CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04812470 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-bde9d58f008049b5a87e5b694854edb9 |
| Source note | uspto-grants-1989_03 |