Реакция #1973927

ord-ab29f206c0b84bf884cdd36779a2db99

Уравнение реакции

[H-].[Na+]
sodium hydride
CC(C)(C)OC(=O)CC(=O)OC(C)(C)C
malonic acid di-tert-butyl ester
[H-].[Na+]
sodium hydride
CCOCC
diethyl ether
O=C1c2ccccc2C(=O)N1CCCCCCCCCCCCBr
4
O=C1c2ccccc2C(=O)N1CCCCCCCCCCCCBr
N-(12-Bromododecyl)phthalimide
CC(C)(C)OC(=O)C(CCCCCCCCCCCCN1C(=O)c2ccccc2C1=O)C(=O)OC(C)(C)C
5c
Выход 67.0%
CC(C)(C)OC(=O)C(CCCCCCCCCCCCN1C(=O)c2ccccc2C1=O)C(=O)OC(C)(C)C
2-(12-phthalimido dodecyl)propane dioic acid di-tert-butyl ester
Выход 67.0%

Растворители

Условия реакции

Температура
75°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеat room temperature
  2. 2
    workup.STIRRINGthe reaction mixture was further stirred at room temperature for 7 h

Методика

29.3 mmol (6.56 mL) of malonic acid di-tert-butyl ester and 29.3 mmol (1.28 g) of sodium hydride in mineral oil (55% (w/w)) were reacted in 120 mL of anhydrous dimethylformamide for 50 min at room temperature according to general procedure B2. 45.4 mmol (23.0 g) of 4′ were added to the mixture and the reaction mixture was stirred for 1 h at 75° C. bath temperature and at room temperature o/n. Additional 16.2 mmol (708 mg) of sodium hydride in mineral oil (55% (w/w)) were added and the reaction mixture was further stirred at room temperature for 7 h. The work-up was performed as described (general procedure B) with diethyl ether. Column chromatography (cyclohexane→cyclohexane/acetone 9:1) gave 5c′ with 67% yield.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08501199B2uspto-grants-2013_08