HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → HCID 54557735, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 20670051 | HCID 20670051 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54557735 | HCID 54557735 | — |
Reaction Steps
Prepared according to the method described in Example 63 from 3- amino-2-chloro-N-(tricyclo[3.3.13,7]dec-1-yl)methylbenzamide from Example 54(0.7 g), 50% chloroacetaldehyde in water (0.353 ml), sodium cyanoborohydride (0.159 g), 50% hydrochloric acid in methanol (0.385 ml) and methanol (10 ml), giving the subtitled compound as a white solid (0.777 g) after purification by flash column chromatography eluting with 3:1 iso-hexane:ethylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06303659B2 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-0aa4451654d6460d8b17387ba6916c6e |
| Source note | uspto-grants-2001_10 |