HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → HCID 20029894, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 20029869 | HCID 20029869 | — |
| Product | HCID 20029894 | HCID 20029894 | — |
Reaction Steps
A mixture of 2,6-dichloro-4-(2,3-epoxypropoxy)benzaldehyde (3 gm) and tert-butylamine (20 ml) is heated at 45° for 17 hours. The excess tert-butylamine is removed under reduced pressure (20 mm). The oil is dissolved in 6 N hydrochloric acid (25 ml) and heated for 1 hour. The acid solution is added to boiling saturated aqueous sodium carbonate with nitrogen ebullition. The basic solution is extracted with chloroform. The chloroform is dried over anhydrous sodium sulfate, filtered and concentrated to 2,6-dichloro-4-(3-tert-butylamino-2-hydroxypropoxy)benzaldehyde which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440774 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-884628990cd2437fa75d0b2827fd34c9 |
| Source note | uspto-grants-1984_04 |