تفاعل #554571

ord-97903a68f3f54b51a3bbcb210323c15d

معادلة التفاعل

COC(=O)CCCCCOC(c1ccccc1)(c1ccccc1)c1ccccc1
15a
COC(=O)CCCCCOC(c1ccccc1)(c1ccccc1)c1ccccc1
Methyl 6-trityloxy-hexanoate
ClC(c1ccccc1)(c1ccccc1)c1ccccc1
Trityl chloride
COC(=O)CCCCCCCCCCCO
14c
COC(=O)CCCCCCCCCCCO
Methyl-12-hydroxy-dodecanoate
COC(=O)CCCCCCCCCCCOC(c1ccccc1)(c1ccccc1)c1ccccc1
pale yellow oil 15c
المردود 40.0%
COC(=O)CCCCCCCCCCCOC(c1ccccc1)(c1ccccc1)c1ccccc1
Methyl-12-trityloxy-dodecanoate
المردود 40.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe filtration step
  2. 2
    أخرىinstead the crude material was purified by flash column chromatography (10% EtOAc in hexanes)

الإجراء التجريبي

The synthesis procedure of 15a was followed. Trityl chloride (1412 mg, 5.1 mmol), 14c (583 mg, 2.5 mmol), and pyridine (10 mL) were used and the reaction was prolonged to 3 days. The filtration step was omitted, instead the crude material was purified by flash column chromatography (10% EtOAc in hexanes) yielding 477 mg (40%) of a pale yellow oil 15c. 1H-NMR (400 MHz, CDCl3, δH ppm): 7.44 (6H, m, p-Ar), 7.28 (6H, m, m-Ar), 7.21 (3H, m, o-Ar), 3.66 (3H, s, CO2CH3), 3.03 (2H, t, 3JH—H=6.6 Hz, H)—CH2), 2.29 (2H, t, 3JH—H=7.5 Hz, CH2CO2), 1.55-1.65 (4H, m, 2CH2), 1.10-1.39 (14H, m, 7CH2). HRMS (EI): m/z calcd 472.2977 (C32H40O3), found 472.2968 [M]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08623326B2uspto-grants-2014_01