Triethylamine → HCID 14349021, compound

HRID 2107702Notes

Reaction equation

HRID 2107702 reaction equation
[NH2:1][CH2:2][CH2:3][N:4]1[CH2:10][CH:9]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][CH:13]=2)[C:8]2[CH:22]=[CH:23][CH:24]=[CH:25][C:7]=2[CH2:6][CH2:5]1.C(N(CC)CC)C.Cl[C:34]([O:36][CH2:37][CH3:38])=[O:35]>C(Cl)(Cl)Cl>[CH2:37]([O:36][C:34]([NH:1][CH2:2][CH2:3][N:4]1[CH2:10][CH:9]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:19])[F:20])=[CH:14][CH:13]=2)[C:8]2[CH:22]=[CH:23][CH:24]=[CH:25][C:7]=2[CH2:6][CH2:5]1)=[O:35])[CH3:38]

Participants

5

Procedure

To a cooled solution of 3-(2-aminoethyl)-2,3,4,5-tetrahydro-1-(p-trifluoromethylphenoxy)-3-benzazepine of Example 21b (5.5 g, 0.016 mole) and triethylamine (1.8 g, 0.018 mole) in chloroform (75 ml) was slowly dropped a solution of ethyl chloroformate (2.0 g, 0.018 mole) in chloroform (25 ml). After stirring twenty hours at ambient temperature the reaction mixture was concentrated to a semisolid which was dissolved in ether, washed with water and dried (saturated NaCl, anhydrous MgSO4). The solution was filtered and concentrated to yield an oil. A sample of the resultant oil was distilled to yield an oil of 3-(2-ethoxycarbonylaminoethyl)-2,3,4,5-tetrahydro-1-(p-trifluoromethylphenoxy)-3-benzazepine, bp 235°-238° C./0.10 mm.

Workup

  1. concentrationwas concentrated to a semisolid which
  2. dissolutionwas dissolved in ether
  3. washwashed with water
  4. dry with materialdried (saturated NaCl, anhydrous MgSO4)
  5. filtrationThe solution was filtered
  6. concentrationconcentrated
  7. customto yield an oil
  8. distillationA sample of the resultant oil was distilled

Sources & evidence

ORD record
ord-8cf567d670b7437aa0fdc7f28e01a086
Source dataset
uspto-grants-1990_06
Patent number
US04935418

Reaction notes

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