HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → (2R)-2-bromo-4-methylpentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | D-Leucine | HCID 439524 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | (2R)-2-bromo-4-methylpentanoic acid | HCID 12697060 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
D-leucine (23.3 g, 177.3 mmol, 1.0 eq) was dissolved into 3.0M HBr in water (280 mL, 840 mmol) and cooled to 0° C. A solution of NaNO2 (19.6 g, 284 mmol) in water (31.9 mL, 1.8 mol) was slowly added over 20 minutes and the mixture was stirred at 0° C. for 3 hours. The mixture was extracted with ethyl ether (2×500 mL), washed with water (100 mL) and saturated aqueous NaCl, dried over MgSO4, filtered, and concentrated, to yield (R)-2-bromo-4-methylpentanoic acid as an off-yellow yellow oil (33.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637562B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-e6c2615bd2c14ee0a4539cb17eb9f840 |
| Source note | uspto-grants-2014_01 |