HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Carboxymethyl 5-amino-4-oxopentanoate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | t-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoate | HCID 90034544 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Carboxymethyl 5-amino-4-oxopentanoate hydrobromide | HCID 90034574 | 92% |
Reaction Steps
A 30% solution of hydrogen bromide in acetic acid (12 mL) was added to the product of 1a (3.3 g; 9.5 mmol) cooled with an ice-water bath and stirred until the oil dissolved with evolution of gas. After stirring for 15 min, the mixture was triturated with hexane (4×20 mL) and diethyl ether (4×20 mL); the oil solidified to a tan powder. The residue was filtered and dried overnight in a drying pistol at ˜50° C. and 12 mm Hg. 4.44 g (92%) product was obtained (tan powder, mp 110-114° C. (dec.)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249086B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-e967cac021ed444685766933b4fc5d22 |
| Source note | uspto-grants-2016_02 |