HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminoacetaldehyde dimethyl acetal → HCID 178495875, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | benzyl N-[(3R)-2-thioxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl]carbamate | HCID 58304042 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178495875 | HCID 178495875 | 92.2% |
Reaction Steps
Combine benzyl N-[(3R)-2-thioxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl]carbamate (8.71 g, 26.68 mmol), mercury dichloride (HgCl2) (9.42 g, 34.69 mmol), and aminoacetaldehyde dimethyl acetal (11.65 mL, 106.73 mmol;) in tetrahydrofuran (250 mL) and heat to 55° C. for 20 minutes. Cool the mixture to ambient temperature and filter it through diatomaceous earth. Wash the cake with THF and ethyl acetate and concentrate the filtrate under reduced pressure. Dissolve the resulting oil in dichloromethane, wash with warm water (4×) and brine, dry over sodium sulfate, and concentrate the organic layer under reduced pressure to give the title compound (9.78 g, 92%) as a solid: MS (m/z): 398 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299061B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-85d580b8a5f9496299af2737d96084c3 |
| Source note | uspto-grants-2012_10 |