تفاعل #554571
ord-97903a68f3f54b51a3bbcb210323c15d
معادلة التفاعل
15a
Methyl 6-trityloxy-hexanoate
Trityl chloride
14c
Methyl-12-hydroxy-dodecanoate
→
pale yellow oil 15c
المردود 40.0%
Methyl-12-trityloxy-dodecanoate
المردود 40.0%
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1ترشيحThe filtration step
- 2أخرىinstead 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]+.