HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976470Generated: October 29, 2026
Triphenylphosphine → HCID 178500271, compound
https://huagongshe.com/reaction/976470
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl 8-bromooctanoate | HCID 11107373 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178500271 | HCID 178500271 | 84.3% |
Reaction Steps
A solution of 8 (1.25 g, 5.23 mmol, 1.0 equiv.) in CH3CN (4.0 mL, 1.31M) was treated with triphenylphosphine (1.50 g, 5.75 mmol, 1.1 equiv.) and stirred at reflux for 10 h. Additional triphenylphosphine (0.685 g, 2.61 mmol 0.5 equiv.) was added to the reaction mixture and stirring was continued at reflux for 5 h. The reaction mixture was concentrated under reduced pressure and washed repeatedly with Et2O (5×10 mL washes). The remaining residue was then solubilized in the minimum volume of CH2Cl2 and concentrated under reduced pressure to afford 9 as a colorless foam (2.20 g, 2.61 g theoretical, 84.3%): 1H NMR (CDCl3, 250 MHz)δ7.82-7.51 (m, 15H, ArH), 3.70-3.46 (m, 5H, CH3OC(O)R and CH2PPh3), 2.13 (t, 2H, J=7.4 Hz, CH2C(O)OCH3), 1.62-1.43 (m, 6H, alkyl protons), 1.30-1.02 (m, 4H, alkyl protons); FABHRMS (NBA) m/e 419.2154 (C27H32BrO2P-Br- requires 419.2140).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05612380 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-138a395c73d94c7cb9b45343979e0ff8 |
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| Source note | uspto-grants-1997_03 |
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