HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 14112562, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Heptenoic acid, methyl ester | HCID 554050 | — |
| Reactant | Diboron | HCID 6328200 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14112562 | HCID 14112562 | — |
Reaction Steps
Compound XL is prepared by reacting endo-bicycle[3.1.0]hex-2-ene-6-carboxylic acid methyl ester with diborane in a mixture of tetrahydrofuran and diethyl ether, a reaction generally known in the art, to give endo-bicyclo[3.100]63 hexan-3-ol-6-carboxylic acid methyl ester which is then reacted with dihydropyran in the presence of a catalytic amount of POCl3 to give the desired compound. This is then used as described in said Belgian patent to produce the endo form of bicyclo-ketone XVI.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983154 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-989b507766c54a2cb7d908e5312409a3 |
| Source note | uspto-grants-1976_09 |