HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentene → HCID 4189396, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentene | HCID 8882 | — |
| Reactant | Diphenylphosphine | HCID 70017 | — |
| Product | HCID 4189396 | HCID 4189396 | — |
Reaction Steps
A stirred mixture of 47.6 g (0.7 m) cyclopentene and 136.7 g (0.735 m) diphenyl phosphine in a quartz wessel was irradiated at 15° C. by a broad spectrum ultraviolet light for 17 days. A slow addition reaction took place. Gas chromatographic analysis indicated 60% conversion at the end of the reaction period. The reaction mixture was then fractionally distilled in vacuo to obtain the desired cyclopentyl diphenyl phoshine adduct as a colorless mobile liquid of bp. 138°-140° C. at 0.3 mm (As a by-product, tetraphenyl biphosphine, bp. 210°-212° C. at 0.15 mm, was obtained.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04593141 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-c29232b6a30a4c55a0428426c8826d96 |
| Source note | uspto-grants-1986_06 |