HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → 3-[3-hydroxy-1,9-dimethoxy-5,9-dimethyl-(E)-decenylidene]-4-butyrolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 20528523 | HCID 20528523 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-[3-hydroxy-1,9-dimethoxy-5,9-dimethyl-(E)-decenylidene]-4-butyrolactone | HCID 86738533 | 63.2% |
Reaction Steps
An etherealdiazomethane solution containing 0.04 moles of diazomethane is added to a solution of 2.0 g (0.006 moles) of 3-(9-methoxy-3-hydroxy-5,9-dimethyl-decanoyl)-4-butyrolactone in 5 ml of dry ether, and the reaction mixture is allowed to stand at room temperature for 4 hours. The solvent is distilled off in vacuo, the residue is taken up with ether, and the solution is filtered through a short column filled with Kieselgel 60 adsorbent. Ether is removed from the effluent to obtain 1.2 g (63.2%) of the aimed compound as a pale yellow oil; Rf =0.62 (developed with a 10:0.4 mixture of benzene and methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04344959 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-ce7495193084499baedc71ddda582255 |
| Source note | uspto-grants-1982_08 |