HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-Chloro-alpha-(4-tert-butoxycarbonylaminomethylphenyl)-2-neopentylaminobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-Amino-5-chloro-alpha-(4-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54502133 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Chloro-alpha-(4-tert-butoxycarbonylaminomethylphenyl)-2-neopentylaminobenzyl alcohol | HCID 54328070 | 100% |
Reaction Steps
To a methanol (8 ml) solution of 2-amino-5-chloro-α-(4-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.83 g) were added trimethyl acetaldehyde (220 mg) and acetic acid (170 mg). The mixture was stirred for 10 minutes at room temperature, to which was added sodium cyano borohydride (160 mg). The mixture was stirred overnight at room temperature, to which was added acetic acid ethyl ester (100 ml). The mixture was washed with water and dried over anhydrous Na2SO4. The solvent was then distilled off, and the residue was purified by means of a silica gel column chromatography to give the object 5-chloro-α-(4-tert-butoxycarbonylaminomethylphenyl)-2-neopentylaminobenzyl alcohol (0.99 g) as a colorless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352982B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-2efdd3ed1c3c4a8c9ffa11aebead2ebf |
| Source note | uspto-grants-2002_03 |