HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-2-methyl-1-propanol → (+/-)-N-(beta-Hydroxy-alpha,alpha-dimethylethyl)-2-[4-(4-chlorophenoxy)-phenoxy]-1-propylamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-2-methyl-1-propanol | HCID 11807 | — |
| Reactant | (+/-)-2-[4-(4-Chlorophenoxy)-phenoxyl]-propyl mesylate | HCID 21318102 | — |
| Solvent | Water | HCID 962 | — |
| Product | (+/-)-N-(beta-Hydroxy-alpha,alpha-dimethylethyl)-2-[4-(4-chlorophenoxy)-phenoxy]-1-propylamine hydrochloride | HCID 21318059 | — |
Reaction Steps
A mixture of 13 g (0.0365 mol) of the mesylate of Example 34 and of 32.5 g (0.365 mol) of 2-amino-2-methyl-1-propanol is heated slowly to 170° C. The reaction mixture is allowed to return to ambient temperature and is taken up in water. The insoluble matter is extracted with diethyl ether and the organic phase obtained is washed with water and dried over dry sodium sulphate to give, after evaporation of the solvent, 12.7 g of a limpid pale yellow oil. After treating 12 g of this oil in a solution of hydrogen chloride in diethyl ether, and purifying the product by crystallisation from ethyl acetate, 11.2 g of a white powder which is soluble in water to the extent of 200 g/l are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156011 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-448834a064344ffd8126315ed70cf19e |
| Source note | uspto-grants-1979_05 |