Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 20029918 | HCID 20029918 | — |
| Product | HCID 20029889 | HCID 20029889 | — |
Reaction Steps
To 4-(2,3-epoxypropoxy)-5,6,7,8-tetrahydronaphthaldehyde (2.4 gms) is added tert.-butylamine (15 ml.). The resulting solution is heated at 45° C. for 15 hours. The excess tert.-butylamine is removed at reduced pressure (20 mm). To the residue is added 30 ml. 6N hydrochloric acid, and the resulting mixture is refluxed for three hours. The acidic mixture i poured into a saturated solution of sodium carbonate which is heated on a steam bath with nitrogen bubbling through it. The basic mixture is extracted with chloroform, which is dried over anhydrous sodium sulfate, filtered and concentrated to give 2.3 g of 4-(3-tert.butylamino-2-hydroxypropoxy)-5,6,7,8-tetrahydronapthaldehyde as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04134983 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-1006e8359d9c4025bc1a438d2fdd2e07 |
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| Source note | uspto-grants-1979_01 |
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