HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester | HCID 22940772 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | N-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanol | HCID 67688130 | — |
Reaction Steps
4.15 g (11.2 mmol) of N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester is dissolved in 20 ml of tert-butyl methyl ether and mixed with 0.17 g (4.5 mmol) of sodium borohydride. At 0° C., 6 ml of methanol is added and it is stirred for three hours under argon at a temperature below 5° C. Then, 0.8 ml of acetic acid, dissolved in 3 ml of tetrahydrofuran, is added, mixed with 3 ml of water and stirred for ten minutes at room temperature. The organic phase is separated, washed with water and dried on sodium sulfate. The drying agent is suctioned off, the filtrate is concentrated by evaporation and the residue is chromatographed for purification on silica gel (eluent: ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05853699 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-ca274c22274d40b7a345efc0e30b3f31 |
| Source note | uspto-grants-1998_12 |