HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 19979960, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(Benzyloxy)benzoic acid | HCID 73880 | — |
| Reactant | Hexyl 2-hydroxypropanoate | HCID 519757 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 19979843 | HCID 19979843 | — |
| Reactant | HCID 19979915 | HCID 19979915 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19979960 | HCID 19979960 | — |
Reaction Steps
A solution of 11.5 g of diethylazodicarboxylate in tetrahydrofuran is added to a mixture of 20.6 g of 4-cyano-4-heptylcyclohexyl p-hydroxybenzoate (obtainable by esterification of 4-cyano-4-heptylcyclohexanol with p-benzyloxybenzoic acid and cleavage of the benzyl group by catalytic hydrogenation), 11.5 g of optically active hexyl lactate and 15.7 g of triphenylphosphine in 150 ml of tetrahydrofuran, stirring is carried out for one hour at 50° and the solvent is removed after 12 hours. The residue is dissolved in 100 ml of hot toluene, cooled down, filtered and the filtrate purified as usual by chromatography and crystallization. Optically active hexyl p-(4-cyano-4-heptylcyclohexyloxycarbonyl)phenoxypropionate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886620 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-c220dfc590ea4c7c87d223c7ac0c7e0b |
| Source note | uspto-grants-1989_12 |