HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → Methyl 2-[(tert-butoxycarbonyl)amino]pent-4-ynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Acetyloxy[[(1,1-dimethylethoxy)carbonyl]amino]acetic acid methyl ester | HCID 10922855 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-[(tert-butoxycarbonyl)amino]pent-4-ynoate | HCID 10537281 | — |
Reaction Steps
To an ice cooled suspension of the product of Example 2 (4.00 g, 16.2 mmol) and zinc dust (2.63 g, 40.5 mmol) in DMF (30 mL) under nitrogen was added slowly via syringe propargyl bromide (80% w/w in toluene) (6.02 g, 40.5 mmol). The bromide was added at such a rate as to maintain the internal temperature between 20°-25° C., then stirred at that temperature for an additional 1 hour. The reaction mixture was diluted with 100 mL of EtOAc, washed successively with 0.5N HCl (200 mL), sat'd NaHCO3 (200 mL) and sat'd NaCl and then dried (MgSO4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05508466 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-26caa51045d747c58e987d743a3649f8 |
| Source note | uspto-grants-1996_04 |