Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 19855578 | HCID 19855578 | — |
| Product | HCID 19855557 | HCID 19855557 | 70% |
Reaction Steps
A solution of 18.0 ml (29.7 g, 0.25 moles) of thionyl chloride in 50 ml of dry benzene is added dropwise, within 0.5 hours, to a suspension of 43.15 g (0.20 moles) of 1-(2,6-dimethylphenyl-amino)-2-propanol hydrochloride in 400 ml of dry benzene. The addition is performed at room temperature under nitrogen atmosphere. The reaction mixture is boiled for 3 hours, then the resulting solution is cooled to room temperature, and 50 ml of water are added dropwise to the mixture at a temperature not exceeding 20° C. Concentrated aqueous ammonia is added then dropwise to the mixture to adjust the pH of the aqueous phase to 9. The phases are separated from each other, and the aqueous phase is extracted twice with 100 ml of benzene, each. The benzene solutions are combined, washed thrice with 100 ml of water, each, dried over anhydrous magnesium sulfate, and the solvent is evaporated. The oily residue is distilled under reduced pressure. 27.6 g (70%) of 1-(2,6-dimethylphenyl)-amino-2-chloro-propane are obtained; b.p.: 99°-100° C./53.3 Pa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04922021 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-8e389ed0c9d649edb69de691b001e81e |
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| Source note | uspto-grants-1990_05 |
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