Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 19915726 | HCID 19915726 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19915718 | HCID 19915718 | — |
Reaction Steps
To a solution of 2-[N-methyl-N-(4-nitrophenethyl)amino]ethanol (8.0 g) in dry methylene chloride (75 ml) was added dropwise thionyl chloride (3ml) with stirring at 0° C. The mixture was allowed to warm to ambient temperature and stirred for 16 hours. The resultant solid was filtered, washed with dry ether and dried to give a colourless product (7.1 g). Crystallisation from ethyl acetate/methanol gave the title compound, 6.0 g, m.p. 168°-169°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05079248 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-356acab45d70431bbbcb455e0a8c0b26 |
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| Source note | uspto-grants-1992_01 |
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