Tert-Butylamine → HCID 20029889, compound

HRID 325348Notes

Reaction equation

HRID 325348 reaction equation
[O:1]1[CH2:17][CH:2]1[CH2:3][O:4][C:5]1[C:14]2[CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[C:8]([CH:15]=[O:16])=[CH:7][CH:6]=1.[C:18]([NH2:22])([CH3:21])([CH3:20])[CH3:19]>>[C:18]([NH:22][CH2:17][CH:2]([OH:1])[CH2:3][O:4][C:5]1[C:14]2[CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[C:8]([CH:15]=[O:16])=[CH:7][CH:6]=1)([CH3:21])([CH3:20])[CH3:19]

Participants

3

Conditions

Temperature
45 °C

Procedure

To 4-(2,3-epoxypropoxy)-5,6,7,8-tetrahydronapthaldehyde (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 is 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.

Workup

  1. customThe excess tert.-butylamine is removed at reduced pressure (20 mm)
  2. additionTo the residue is added 30 ml
  3. temperature6N hydrochloric acid, and the resulting mixture is refluxed for three hours
  4. additionThe acidic mixture is poured into a saturated solution of sodium carbonate which
  5. temperatureis heated on a steam bath with nitrogen bubbling through it
  6. extractionThe basic mixture is extracted with chloroform, which
  7. dry with materialis dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-0247fc3093bf410db2e6f1d1d86f0a56
Source dataset
uspto-grants-1984_04
Patent number
US04440774

Reaction notes

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