反応 #1810791

ord-f53083cc4a4d49238dacc84eedf1a2d3

反応方程式

[Na]
sodium
O=C(O)CCCO
4-hydroxybutyric acid
O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
C(=NC1CCCCC1)=NC1CCCCC1
N,N′-dicyclohexylcarbodiimide
COc1ccc(C(Cl)(c2ccccc2)c2ccc(OC)cc2)cc1
4,4′-dimethoxytrityl chloride
COc1ccc(C(OCCCC(=O)Oc2ccc([N+](=O)[O-])cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
desired compound
COc1ccc(C(OCCCC(=O)Oc2ccc([N+](=O)[O-])cc2)(c2ccccc2)c2ccc(OC)cc2)cc1
4-Nitrophenyl 4-(4,4′-dimethoxytrityloxy)butyrate

溶媒

反応条件

温度
22°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The precipitated dicyclohexylurea is filtered off
  2. 2
    洗浄washed with dichloromethane
  3. 3
    濃縮The filtrate is concentrated
  4. 4
    その他The residue is purified on a silica gel column (10-50% ethyl acetate and 1% triethylamine in petroleum ether)

実験手順

The sodium salt of 4-hydroxybutyric acid (1.26 g; 10 mmol) is dissolved in anhydrous pyridine (30 ml), and 4,4′-dimethoxytrityl chloride (3.39 g; 3.05 mmol) is added. After 16 hours, 4-nitrophenol (1.39 g; 10 mmol) and N,N′-dicyclohexylcarbodiimide (2.06 g; 10 mmol) are added, and the mixture is stirred at 22° C. for a further 48 hours. The precipitated dicyclohexylurea is filtered off and washed with dichloromethane. The filtrate is concentrated and the resulting residue is coevaporated twice with toluene. The residue is purified on a silica gel column (10-50% ethyl acetate and 1% triethylamine in petroleum ether). The desired compound is obtained in the form of a pale yellowish-colored oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07485421B2uspto-grants-2009_02