HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → (2R,3S)-2-Bromo-3-methylpentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | D-Alloisoleucine | HCID 94206 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R,3S)-2-Bromo-3-methylpentanoic acid | HCID 51381013 | 87.5% |
Reaction Steps
The (2R,3S)-2-amino-3-methylpentanoic acid (D-allo-isoleucine, 1g, 7.62 mmol) was dissolved in a mixture of HBr 48% (6.95 mL, 61 mmol) and H2O (10.5 mL). At 0° C., a solution of NaNO2 (1.68 g, 24.4 mmol) in H2O (5 mL) was added over a period of 30 min. The reaction was stirred for two hours. The reaction mixture was degassed in vacuo and extracted with EtOAc (2×20mL). The extracts were washed with water (15 mL), dried (Na2SO4), filtered and evaporated to give 1.3 g (87% yield) of the (2R, 3S)-2-bromo-3-methylpentanoic acid as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390789B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-20ad5afcb6474824bde3777d88952182 |
| Source note | uspto-grants-2008_06 |