HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 54486441, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Cyclohexylacetyl chloride | HCID 2757989 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54486441 | HCID 54486441 | — |
Reaction Steps
A solution of 19.8 g of cyclohexylacetyl chloride (b.p. 98° - 100°/23 mm Hg) in 150 ml of dry ether is slowly added at 0°-5° with cooling in an ice-water bath to a vigorously stirred solution of 11 g of diazomethane in 500 ml of ether. The excess diazomethane and ether is distilled off under reduced pressure and cyclohexylmethyl diazomethyl ketone is obtained as residue; infra-red absorption spectrum (in methylene chloride): characteristic bands at 3.45μ, 3.52μ, 4.75μ and 6.12μ; the product is processed without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052408 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-5fc8cf98eb96412287556abac7d6bebb |
| Source note | uspto-grants-1977_10 |