HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → HCID 13457778, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Benzyl azepane-3-carboxylate | HCID 13457777 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13457778 | HCID 13457778 | — |
Reaction Steps
To a solution of 1.46 g 3-benzyloxycarbonylperhydroazepine and 1.06 g methvl bromoacetate in 30 ml benzene add 1.06 g silver oxide. Stir the reaction in the dark for 24 hr., filter and concentrate the filtrate in vacuo. Dissolve the residue in HCl (pH 1.5) and wash the solution with ether. Make the aqueous phase to pH 12 and extract with ethyl acetate. Dry and concentrate the extracts to obtain 1-methoxycarbonylmethyl-3-benzyloxycarbonylperhydroazepine. NMR (CDCl3, TMS)-δ 1.8 ;(m, 6H); δ 2.8 (m, 2H); δ 3.1 (d, 2H); δ 3.45 (s, 2H); δ 3.65 (s, 3H); δ 5.15 (s, 2H); δ 7.3 (s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04520021 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-a99cca3ed5b945f79e137ad8390b60e8 |
| Source note | uspto-grants-1985_05 |