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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976470Generated: October 29, 2026

Triphenylphosphine → HCID 178500271, compound

https://huagongshe.com/reaction/976470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 8-bromooctanoateHCID 11107373—
SolventAcetonitrileHCID 6342—
ProductHCID 178500271HCID 17850027184.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612380
Source datasetuspto-grants-1997_03
ORD IDord-138a395c73d94c7cb9b45343979e0ff8
Source noteuspto-grants-1997_03