Reaktion #8283

ord-b7d7674ad59d4f66821709f6ec79f701

Reaktionsgleichung

CCOC(=O)CCC(O)CO
4,5-dihydroxy-pentanoic acid ethyl ester
CC(C)(C)[Si](C)(C)Cl
tert-butyl-dimethyl-silyl chloride
CCN(CC)CC
triethylamine
CCOC(=O)CCC(O)CO[Si](C)(C)C(C)(C)C
title compound
CCOC(=O)CCC(O)CO[Si](C)(C)C(C)(C)C
5-(tert-Butyl-dimethyl-silyloxy)-4-hydroxy-pentanoic acid ethyl ester

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with water (100 mL), saturated ammonium chloride solution, and brine
  2. 2
    FiltrationThe solution is filtered
  3. 3
    Einengenconcentrated in vacuo

Vorschrift

A solution of 4,5-dihydroxy-pentanoic acid ethyl ester, (7 g, 43.2 mmol) and 4-dimethylaminopyridine (0.2 g, 1.73 mmol) in dichloromethane (145 mL) at room temperature under nitrogen is treated with tert-butyl-dimethyl-silyl chloride (7.8 g, 51.85 mmol) and triethylamine (6.9 mL, 47.52 mmol) and stirred 18 h. The mixture is diluted with dichloromethane (100 mL), washed with water (100 mL), saturated ammonium chloride solution, and brine. The solution is filtered and concentrated in vacuo to yield the title compound, 11.85 g (99%), as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087626B2uspto-grants-2006_08