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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976472Generated: October 26, 2026

Triphenylphosphine → HCID 178500264, compound

https://huagongshe.com/reaction/976472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 9-bromononanoateHCID 554142—
SolventAcetonitrileHCID 6342—
ProductHCID 178500264HCID 17850026491.3%

Reaction Steps

A solution of 13 (1.02 g, 4.06 mmol, 10 equiv) in CH3CN (3.5 mL 1.16M) was treated with triphenylphosphine (1.17 g, 4.47 mmol, 1.1 equiv) and stirred at reflux for 10 h. Additional triphenylphosphine (0.532 g, 2.03 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 14 as a colorless foam (1.90 g, 2.08 g theoretical, 91.3%): 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), 1.62-1.02 (m, 12H, alkyl protons); FABHRMS (NBA) m/e 433.2312 (C28H34BrO2P--Br- requires 433.2296).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612380
Source datasetuspto-grants-1997_03
ORD IDord-c6f2b19c1a1440289099bac653c68927
Source noteuspto-grants-1997_03