Basic information Safety Supplier Related

(S)-(+)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLIC ACID

Basic information Safety Supplier Related

(S)-(+)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLIC ACID Basic information

Product Name:
(S)-(+)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLIC ACID
Synonyms:
  • (S)-(+)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLIC ACID
  • (S)-2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID
  • (S)-(+)-DMCPCA
  • (S)-(+)-2,2-Dimethylcyclopropanecarboxylic Acid
  • (1S)-2,2-dimethylcyclopropane-1-carboxylic acid
  • (S)-(+)-2,2-DimethylcyclopropanecarboxylicAcid>
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-, (1S)-
  • (S)-2,2-Dimethyl cycolpropanecarboxylic acid
CAS:
14590-53-5
MF:
C6H10O2
MW:
114.14
Product Categories:
  • Carboxylic Acids (Chiral)
  • Chiral Building Blocks
  • Cyclopropanes
  • Simple 3-Membered Ring Compounds
  • Synthetic Organic Chemistry
Mol File:
14590-53-5.mol
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(S)-(+)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLIC ACID Chemical Properties

Boiling point:
100 °C / 12mmHg
Density 
0.99
refractive index 
124 ° (C=1, MeOH)
storage temp. 
Sealed in dry,Room Temperature
pka
4.99±0.22(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

HS Code 
2916200090
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(S)-(+)-2,2-DIMETHYLCYCLOPROPANE CARBOXYLIC ACID Usage And Synthesis

Synthesis

645413-67-8

14590-53-5

General procedure for the synthesis of (S)-(+)-2,2-dimethylcyclopropanecarboxylic acid from 2,2,2-difluorocyclopropanecarboxylic acid 2,2-difluoroethyl ester (60 g): in a 2L round-bottomed flask equipped with a stirrer, a pH meter, and a thermometer, 2,2,2-difluorocyclopropanecarboxylic acid 2,2-difluoroethyl ester (60 g), potassium hydrogen phosphate (2 mg) and water (600 mL) were added. Esterase (CLS-BC-21012, 1.5 g) was added to the reaction mixture and the reaction temperature was maintained at 40 °C. The pH of the reaction system was adjusted to 7.0 using 50% aqueous sodium bicarbonate.After the reaction was completed, the esterase was removed by filtration through filter paper, and 35% hydrochloric acid was slowly added to the filtrate to adjust the pH to 2.0.Subsequently, ethyl acetate (600 mL) was added to the mixture, and it was stirred for 15 min. The organic and aqueous phases were separated, and the organic phase was distilled to recover the solvent and low-boiling organics to afford (S)-(+)-2,2-dimethylcyclopropanecarboxylic acid (Yield: 49.1%, Purity: 99.0%, Optical purity: 99.1%). tlc Rf = 0.5 (n-hexane/ethyl acetate, 2:1). 1H NMR (CDCl3, 300MHz) δ: 1.55 ( dd, 1H, J = 7.95Hz, J = 5.42Hz), 1.19 (s, 3H), 1.16 (s, 3H), 1.13 (dd, 1H, J = 4.98Hz, J = 4.89Hz), 0.92 (dd, 1H, J = 7.98Hz, J = 4.42Hz).

References

[1] Patent: WO2004/5241, 2004, A1. Location in patent: Page 9-10

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