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HRID 976472作成日:2026年10月24日

Triphenylphosphine → HCID 178500264、化合物

https://huagongshe.com/ja/reaction/976472

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Methyl 9-bromononanoateHCID 554142—
溶媒AcetonitrileHCID 6342—
生成物HCID 178500264HCID 17850026491.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05612380
出典データセットuspto-grants-1997_03
ORD IDord-c6f2b19c1a1440289099bac653c68927
出典メモuspto-grants-1997_03