HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 136409723, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | HCID 70633857 | HCID 70633857 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 136409723 | HCID 136409723 | — |
Reaction Steps
A mixture of 2.5 g. (5.9 millimols) of (R)-2-amino-1,1-di(2-isopropoxyphenyl)-3-phenyl-1-propanol {[α]D +65.0° (c 1.0, chloroform)} and 0.66 g. (5.4 millimols) of salicylaldehyde in 50 ml benzene was heated under reflux for 2.5 hours. After the distillation of the solvent from the reaction mixture, the residue was recrystallized from ethanol to give (R)-N-salicylidene-2-amino-1,1-di(2-isopropoxyphenyl)-3-phenyl-1-propanol as yellow crystals. Yield, 2.43 g. (85%); melting point, 152° - 153° C.; [α]D, +65.25° (c 1.00, chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029683 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-a458efc6bb7a41e48611c0ff2f3bf502 |
| Source note | uspto-grants-1977_06 |