tert-butyl cyclopropanecarboxylate
tert-butyl cyclopropanecarboxylate Basic information
- Product Name:
- tert-butyl cyclopropanecarboxylate
- Synonyms:
-
- tert-butyl cyclopropanecarboxylate
- Cyclopropanecarboxylic acid, 1,1-dimethylethyl ester
- 2-ethyl-, 1,1-dimethylethyl ester, (2R)-1-Pyrrolidinecarboxylic acid,
- 1,1-Dimethylethyl cyclopropanecarboxylate
- tert-Butyl cyclopropan-carboxylate
- CAS:
- 87661-20-9
- MF:
- C8H14O2
- MW:
- 142.2
- Mol File:
- 87661-20-9.mol
tert-butyl cyclopropanecarboxylate Chemical Properties
- Boiling point:
- 154 °C
- Density
- 1.012±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- form
- liquid
- color
- Colourless
- InChI
- InChI=1S/C8H14O2/c1-8(2,3)10-7(9)6-4-5-6/h6H,4-5H2,1-3H3
- InChIKey
- FTEAAYMAQFBUJJ-UHFFFAOYSA-N
- SMILES
- C1(C(OC(C)(C)C)=O)CC1
tert-butyl cyclopropanecarboxylate Usage And Synthesis
Synthesis
865-47-4
4023-34-1
87661-20-9
219.1 g (1913 mmol, 1 eq.) of potassium tert-butoxide was suspended in 2.5 L of tert-butyl methyl ether and the mixture was cooled to 0-5 °C. 200 g (1913 mmol, 1 eq.) of cyclopropanecarbonyl chloride was added slowly and dropwise over 60 min while maintaining the reaction temperature between 0-5 °C (cooled using an ice-ethanol bath). The progress of the reaction was monitored by on-line FTIR to ensure that the reaction was carried out in a controlled manner. The reaction mixture was continued to be stirred at 0-5 °C for 30 min before being neutralized by adding 1 L of 5% aqueous sodium bicarbonate solution. The aqueous phase was separated and the aqueous phase was extracted with 500 mL of tert-butyl methyl ether. The organic phase was combined and washed with 500 mL of half-saturated aqueous sodium chloride solution. The organic phase was concentrated under reduced pressure (30 °C/150 mbar) to give 271 g of tert-butyl cyclopropanecarboxylate (91% yield, containing 8% residual tert-butyl methyl ether).
References
[1] Patent: US2009/23713, 2009, A1. Location in patent: Page/Page column 20
[2] Patent: US2010/22518, 2010, A1. Location in patent: Page/Page column 20
[3] Patent: US2010/16282, 2010, A1. Location in patent: Page/Page column 19
[4] Patent: US2011/92698, 2011, A1. Location in patent: Page/Page column 22
[5] Journal of Organic Chemistry, 2009, vol. 74, # 22, p. 8726 - 8732
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