Sodium Bicarbonate → 1R-cis-Permethrinic acid

HRID 323923Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 323923
[CH3:1][C:2]1([CH3:13])[C@H:7]2[C@@H:3]1[C@H:4]([C:9](Cl)([Cl:11])[Cl:10])[O:5][C:6]2=[O:8].CC1(C)[C@H]2[C@@H]1[C@@H](C(Cl)(Cl)Cl)OC2=O.C(=O)([O-])O.[Na+].Cl.C(OC)(C)(C)C>CN(C=O)C>[Cl:10][C:9]([Cl:11])=[CH:4][C@H:3]1[C@@H:7]([C:6]([OH:8])=[O:5])[C:2]1([CH3:1])[CH3:13]

Komponenten

6

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A mixture of (1R,4R,5S)-6,6-dimethyl-4-(trichloromethyl)-3-oxabicyclo[3.1.0]hexan-2-one (I, R1=X1=X2=Cl) and (1R,4S,5S)-6,6-dimethyl-4-(trichloromethyl)-3-oxabicyclo[3.1.0]hexan-2-one (I, R1=X1=X2=Cl), 0.24 g (0.001 mol), is stirred with sodium hydrogen carbonate, 0.21 g (0.0025 mol), and Pd(C) 5%, 0.01 g, in about 4 ml of DMF at 50° C. under a hydrogen atmosphere of a slight overpressure. After stirring for ½ hour at 50° C. the mixture is stirred at room temperature. Samples taken out for GC analysis are treated with aqueous hydrochloric acid/methyl t-butyl ether and analysed on GC. After 16 hours GC analysis (area-%) shows a content of 39% of II and 32% of unreacted I. The retention time is identical to that of II prepared according to Ref.6, and MS (Mass (intensity in % of base peak): 208 (6) M+, 210 (4) (M+2)+, 175 (25), 173 (78), 165 (27), 163 (39), 111 (22), 109 (28), 91 (100), 77 (46), 39 (64)) is identical to MS of II prepared according to Ref.6.

Aufarbeitung

  1. stirringis stirred at room temperature
  2. waitAfter 16 hours GC analysis (area-%) shows
  3. customprepared
  4. customprepared

Quellen und Nachweise

ORD-Eintrag
ord-da76437e83b4464dac9176e69f47776c
Quelldatensatz
uspto-grants-2001_04
Patentnummer
US06215023B1

Notizen zur Reaktion

Wird geladen…