Benzyl bromoacetate → Benzyl 2-hydroxyacetate

HRID 241547

Reaktionsgleichung

Reaktionsgleichung von HRID 241547
Br[CH2:2][C:3]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4].C1(C)C=CC=CC=1.C([O:22]CC)C>C(Cl)(Cl)Cl.C(#N)C.C(=O)([O-])[O-].[Ag+2]>[C:3]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:4])[CH2:2][OH:22]

Komponenten

6

Versuchsvorschrift

To a mixture of pentanoracid 7 (600 mg; 1.2 mmol), silver carbonate (440 mg; 1.6 mmol) in a mixture of chloroform (10 ml) and acetonitrile (7 ml), benzyl bromacetate (260 μl; 1.6 mmol) was added and the reaction mixture was stirred for 28 hours at room temperature. The course of the reaction was monitored by TLC (toluene/diethyl ether 6:1). The reaction mixture was then filtered through diatomaceous earth and the filtrate was worked-up and the product was purified by analogical procedure as in the preparation of 21-oxoacid benzyl glycolate. The obtained crude pentanoracid benzyl glycolate (358 mg; 46%) having m.p. 156-157° C. (methanol), [α]D=+57° (c=0.31) was used in the next step.

Aufarbeitung

  1. additionwas added
  2. filtrationThe reaction mixture was then filtered through diatomaceous earth
  3. customthe product was purified by analogical procedure as in the preparation of 21-oxoacid benzyl glycolate

Quellen und Nachweise

ORD-Eintrag
ord-ad35902827f84728ac84b2bd8c661cb4
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08653056B2

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