Реакция #1502

ord-169f88b27a294c15b3d94e8de0e682c6

Уравнение реакции

O=C(Cl)OCCl
Chloromethyl chloroformate
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
cholesterol
c1ccncc1
Pyridine
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
3-(Chloromethoxycarbonyl) Cholesterol

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe solution was cooled
  2. 2
    ТемператураHeat
  3. 3
    Другоеwas produced
  4. 4
    Другоеthe reaction gave a clear solution from
  5. 5
    Промывкаwashed with 0.5M HCl (50 ml) and water (3×25 ml)
  6. 6
    ДругоеAfter treatment with MgSO4, the solution was evaporated to dryness

Методика

Chloromethyl chloroformate (1.96 g, 15.2 mmol) and cholesterol (5.0 g, 12.9 mmol) was dissolved in CH2Cl2 (10 ml). The solution was cooled. Pyridine (1.21 g, 15.3 mmol) was dripped into the stirred solution over 5 minutes. Heat was produced and the reaction gave a clear solution from a somewhat unclear starting solution. After 24 hours at room temperature, the mixture was diluted with CH2Cl2 (50 ml), washed with 0.5M HCl (50 ml) and water (3×25 ml). After treatment with MgSO4, the solution was evaporated to dryness.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05725840uspto-grants-1998_03