HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (R)-2-(2-bromo-3-methylbutyryl)amino-6-isopropylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Amino-6-isopropylphenol hydrochloride | HCID 21293037 | — |
| Reactant | (R)-2-bromo-3methylbutyryl chloride | HCID 22839824 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-2-(2-bromo-3-methylbutyryl)amino-6-isopropylphenol | HCID 6932486 | 76.1% |
Reaction Steps
To a stirred, ice-cooled mixture of 2-amino-6-isopropylphenol hydrochloride (15.0 g), ethyl acetate (200 ml), water (100 ml), and sodium bicarbonate (20.0 g), was added dropwise a solution of (R)-2-bromo-3methylbutyryl chloride (16.0 g) in ethyl acetate (30 ml). The whole was stirred for 30 minutes, and the ethyl acetate layer was separated, washed with water and dried over MgSO4. Removal of the solvent gave (R)-2-(2-bromo-3-methylbutyryl)amino-6-isopropylphenol as crystals (19.1 g, 76.1%). Recrystallization from isopropyl ether afforded colorless needles, mp 108°-109° C. [α]D23 +44.8° (c=0.82, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04771050 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-2f24d0c71b41437d93d6c3ff70833fcb |
| Source note | uspto-grants-1988_09 |