Ethyl 3-bromopropionate
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| Names | |
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| Preferred IUPAC name Ethyl 3-bromopropanoate | |
| Other names Ethyl β-Bromopropionate, Ethyl 2-bromopropanoate | |
| Identifiers | |
3D model (JSmol) | |
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| Properties | |
| C5H9BrO2 | |
| Molar mass | 181.029 g·mol−1 |
| Appearance | colorless liquid |
| Density | 1.4409 g/cm3 |
| Boiling point | 135–136 °C (275–277 °F; 408–409 K) 50 mmHg |
| Hazards | |
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| Warning | |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Ethyl 3-bromopropionate is the organobromine compound with the formula BrCH2CH2CO2C2H5. It is a colorless liquid and an alkylating agent. It is prepared by the esterification of 3-bromopropionic acid.[1] Alternatively, it can be prepared by hydrobromination of ethyl acrylate, a reaction that proceeds in an anti-Markovnikov sense.[2]
See also
References
- ^ Kendall, E. C.; McKenzie, B. (1923). "Ethyl β-Bromopropionate". Organic Syntheses. 3: 51. doi:10.15227/orgsyn.003.0051.
- ^ Mozingo, Ralph; Patterson, L. A. (1940). "Methyl β-Bromopropionate". Organic Syntheses. 20: 64. doi:10.15227/orgsyn.020.0064.

