HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-1-(4-benzyloxyphenyl)ethanol → HCID 53959586, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-1-(4-benzyloxyphenyl)ethanol | HCID 423990 | — |
| Reactant | 2,3-dihydro-2,2-dimethyl-6-(2-oxopropoxy)-4H-1,3-benzoxazin-4-one | HCID 13754332 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53959586 | HCID 53959586 | — |
Reaction Steps
A solution of 9.6 g of 2,3-dihydro-2,2-dimethyl-6-(2-oxo-propoxy)-4H-1,3-benzoxazin-4-one and 9.37 g of 4-benzyloxy-α-(aminomethyl)benzyl alcohol in 250 ml of methanol is hydrogenated analogously to Example 1 until one equivalent of hydrogen has been taken up. The catalyst is filtered off and, after adding 40 ml of isopropylamine, the solution is refluxed for 1 hour. Evaporation of the reaction mixture yields 4-benzyloxy-α-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-1-methyl-ethyl]-aminomethyl-benzyl alcohol in the form of a crystalline mass which can be hydrogenated without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04460580 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-054b35ec5d1e4bcfb8ee98c07ce1bf54 |
| Source note | uspto-grants-1984_07 |