Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorodiphenylphosphine | HCID 66180 | — |
| Reactant | HCID 22648423 | HCID 22648423 | — |
| Reactant | HCID 86591154 | HCID 86591154 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22648420 | HCID 22648420 | 61% |
Reaction Steps
To a solution of 1.31 g (4.5 mmole)2-[4-methyl-2-(1-phenyl-vinyl)-phenoxymethyl]-pyrrolidine and 1.13 g (11.2 mmole) triethylamine in 12 ml abs. toluene at 0° within 30 minutes 1.00 g (4.6 mmole) P-chlorodiphenylphosphine in 3 ml abs. toluene are added dropwise. The reaction solution is left under agitation at RT for 20 h. Then the resultant triethylammonium chloride is filtered off, the residue is recleaned with 20 ml toluene and the filtrate is reduced on the rotary evaporator. Cleaning of the raw product obtained takes place by column chromatography on silica gel with MTBE/cyclohexane/diisopropylamine (ratio of volumes=5/1+10 Vol−%) as the eluant. 1.31 g (2.7 mmole, 61%)diphenylphosphanyl-[4-methyl-2-(1-phenyl-vinyl)-phenoxymethyl]-pyrrolidine are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809225B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-d7ecac4fe6ca4620a9cdd0a56c522f8a |
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| Source note | uspto-grants-2004_10 |
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