Реакция #816393

ord-4e8632ed821d4130ac3598ea3934cfda

Уравнение реакции

Cc1ccc(S(=O)(=O)C(O)(O)CC(C)CCCC(C)CCCC(C)CCCC(C)C)cc1
phytandiol
Cc1ccc(S(=O)(=O)C(O)(O)CC(C)CCCC(C)CCCC(C)CCCC(C)C)cc1
para-toluene sulfonyl phytandiol
[N-]=[N+]=[N-].[Na+]
sodium azide
[N-]=[N+]=[N-]
azide
CC(C)CCCC(C)CCCC(C)CCCC(C)CC(O)(O)N=[N+]=[N-]
azido phytandiol
Выход 81.6%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураby reflux for 5 hr in order
  2. 2
    ЭкстракцияThe reaction mixture was extracted with 50 ml of methylene chloride solution
  3. 3
    Промывкаwashed with saline
  4. 4
    СушкаFollowing drying over anhydrous magnesium sulfate, filtration and concentration

Методика

The yielded phytandiol derivative (0.48 g) was dissolved in 25 ml of dimethyl formamide and 0.06 g (1.00 mmol) of sodium azide (Sigma-Aldrich) was added, followed by reflux for 5 hr in order to substitute azide for para-toluene sulfonyl group. The reaction mixture was extracted with 50 ml of methylene chloride solution and washed with saline. Following drying over anhydrous magnesium sulfate, filtration and concentration, 0.29 g of azido phytandiol derivative was yielded.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07582306B2uspto-grants-2009_09