HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 54330669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 14484454 | HCID 14484454 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54330669 | HCID 54330669 | 100% |
Reaction Steps
A solution of 1-benzoyloxycyclohex-4-ene-2-carboxylic acid (5, 160 mg, 0.645 mmol) in ether (5 ml) is treated with a solution of diazomethane (excess) in ether. The solvent was removed under vacuum to yield methyl cis-2-benzoyloxy-cyclohex-4-enecarboxylate (6, 168 mg, 100%) as a colorless oil. When enantiomerically pure starting material was used, the product of this reaction was >97% enantiomerically pure. [α]D (c 6.35, acetone)=-89.5 for the 1S,2R isomer).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05216141 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-22fe9205315a45869da6548137814bc3 |
| Source note | uspto-grants-1993_06 |