HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → (S)-(+)-2-Amino-4-bromobutyric Acid Hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | L-Homoserine lactone | HCID 445963 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (S)-(+)-2-Amino-4-bromobutyric Acid Hydrobromide | HCID 2733672 | 98% |
Reaction Steps
(S)-3-aminodihydrofuran-2(3H)-one hudrochloride (10.30 g, 74.87 mmol) in 58 mL of 30% w/w HBr in HOAc was stirred at 65° C. for 30 hrs. The solvent was removed under reduced pressure and the resulted solid was suspended in MTBE (200 mL) and stirred for 30 min. The solid was collected by filtration and washed with MTBE (200 mL) and dried to give (S)-2-amino-4-bromobutanoic acid hydrobromide as white solid (19.33 g, 98%). 1H NMR (400 MHz, d6-DMSO) δ 8.37 (s, 3H), 4.01 (m, 1H), 3.65 (m, 2H), 2.33 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299021B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-8d1d6032ea494fb1b7952270ba46c5f5 |
| Source note | uspto-grants-2012_10 |