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| | 1-(2-Chloroethyl)pyrrolidine Hydrochloride Basic information |
| | 1-(2-Chloroethyl)pyrrolidine Hydrochloride Chemical Properties |
| Melting point | 167-170 °C(lit.) | | Boiling point | 237°C(lit.) | | density | 0.4[at 20℃] | | vapor pressure | 1.64hPa at 25℃ | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Chloroform (Slightly), Water (Slightly) | | form | Crystalline Powder or Crystals | | color | White to off-white | | Water Solubility | Soluble | | Sensitive | Hygroscopic | | BRN | 3677061 | | InChI | InChI=1S/C6H12ClN.ClH/c7-3-6-8-4-1-2-5-8;/h1-6H2;1H | | InChIKey | FSNGFFWICFYWQC-UHFFFAOYSA-N | | SMILES | N1(CCCl)CCCC1.[H]Cl | | LogP | 0.736 at 25℃ | | CAS DataBase Reference | 7250-67-1(CAS DataBase Reference) |
| | 1-(2-Chloroethyl)pyrrolidine Hydrochloride Usage And Synthesis |
| Chemical Properties | white to off-white crystals or crystalline powder | | Uses | 1-(2-Chloroethyl)pyrrolidine is a haloalkyl substituted pyrrolidine used in the preparation of various pharmaceutical compound such as the estrogen receptor antagonist Nafoxidine (N212800) and its ana
logues. | | Uses | 1-(2-Chloroethyl)pyrrolidine is a haloalkyl substituted pyrrolidine used in the preparation of various pharmaceutical compound such as the estrogen receptor antagonist Nafoxidine (N212800) and its analogues. | | Purification Methods | Purify the hydrochloride by recrystallisation from isopropanol/di-isopropyl ether (charcoal) and recrystallise it twice more. The free base, b 55-56o/11mm, 60-63o/23mm and 90o/56mm, is relatively unstable and should be converted to the hydrochloride immediately, by dissolving in isopropanol and bubbling dry HCl through the solution at 0o, filtering off the hydrochloride and recrystallising it. The picrate has m 107.3-107.8o (from EtOH) [Cason J Org Chem 24 247 1959, Wright et al. J Am Chem Soc 70 3098 1948]. [Beilstein 20 III/IV 66.] |
| | 1-(2-Chloroethyl)pyrrolidine Hydrochloride Preparation Products And Raw materials |
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