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15224-11-0

15224-11-0 Structure

15224-11-0 Structure
IdentificationBack Directory
[Name]

2-HYDROXYMETHYL-CYCLOPROPANECARBOXYLIC ACID ETHYL ESTER
[CAS]

15224-11-0
[Synonyms]

Ethyl 2-(hydroxyMethyl)cyclopropanecarboxylate
ethyl 2‐(hydroxymethyl)cyclopropane‐1‐carboxylate
trans-ethyl 2-hydroxymethyl-1-cyclopropanecarboxylate
Cyclopropanecarboxylic acid, 2-(hydroxymethyl)-, ethyl ester
[Molecular Formula]

C7H12O3
[MDL Number]

MFCD06202758
[MOL File]

15224-11-0.mol
[Molecular Weight]

144.17
Chemical PropertiesBack Directory
[Boiling point ]

205.9±13.0 °C(Predicted)
[density ]

1.144±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

15.10±0.10(Predicted)
[Appearance]

colourless to yellow liquid
Spectrum DetailBack Directory
[Spectrum Detail]

2-HYDROXYMETHYL-CYCLOPROPANECARBOXYLIC ACID ETHYL ESTER(15224-11-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

(1R,2R)-ethyl 2-formylcyclopropanecarboxylate

13949-93-4

2-HYDROXYMETHYL-CYCLOPROPANECARBOXYLIC ACID ETHYL ESTER

15224-11-0

Step 1: To a solution of ethyl rel-(1R,2R)-2-formylcyclopropanecarboxylate (2.00 g, 13.68 mmol) in anhydrous ethanol (55.0 mL) was added sodium borohydride (0.776 g, 20.53 mmol) in one portion at room temperature and anhydrous conditions. The reaction mixture was stirred at room temperature for 5 h. Subsequently, the reaction was quenched with phosphate buffer aqueous solution (100 mL) at pH 7 and the ethanol was removed by distillation under reduced pressure. The remaining aqueous phase was decanted with dichloromethane (100 mL) followed by further extraction with dichloromethane (2 x 100 mL). The organic phases were combined and washed sequentially with phosphate buffered aqueous solution (70 mL) and saturated saline (70 mL) at pH 7. After drying with anhydrous magnesium sulfate, the product was filtered and concentrated to afford ethyl 2-(hydroxymethyl)cyclopropanecarboxylate (C-5) as a light-yellow oil (1.334 g, 68% yield), which was ready for use in the subsequent steps without further purification. Mass spectrometry analysis showed [M + 1] peak: m/e 145.

[References]

[1] Patent: WO2005/23818, 2005, A2. Location in patent: Page/Page column 136
[2] Patent: US2011/224137, 2011, A1
[3] Patent: WO2011/106273, 2011, A1. Location in patent: Page/Page column 71; 72
[4] Patent: WO2011/53519, 2011, A1. Location in patent: Page/Page column 26
[5] Patent: WO2013/170030, 2013, A1. Location in patent: Page/Page column 75
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