Ethanol → HCID 21402927, compound

HRID 1287632Notes

Reaction equation

HRID 1287632 reaction equation
[CH:1]1[C:11]2[CH2:10][CH:9]([CH2:12][NH2:13])[C:8]3[CH:14]=[CH:15][CH:16]=[CH:17][C:7]=3[CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[C:18]1(=[O:24])[O:23][CH2:22][CH2:21][CH2:20][CH2:19]1.C(O)C.C(=O)([O-])[O-].[K+].[K+]>O>[CH:1]1[C:11]2[CH2:10][CH:9]([CH2:12][NH:13][C:22](=[O:23])[CH2:21][CH2:20][CH2:19][CH2:18][OH:24])[C:8]3[CH:14]=[CH:15][CH:16]=[CH:17][C:7]=3[CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1

Participants

6

Conditions

Temperature
60 °C

Procedure

10,11-Dihydro-5H-dibenzo[a,d]cycloheptene-10-methylamine, γmaxCHCl3 3390, 3300 cm-1, (52.3 g, 0.234 mole), is combined with δ-valerolactone (35 g, 0.35 mole). The mixture is heated for 2 hr. at 150° C (oil bath temperature). After partial cooling, ethanol (250 ml) is added followed by a solution of potassium carbonate (50 g, 0.36 mole) in water (150 ml). The two-phase mixture is stirred at 60° C overnight. The ethanol is removed under reduced pressure and the residual mixture extracted with chloroform. The chloroform solution is washed with water, dried and taken to dryness. The residue is crystallized from benzene (750 ml) -ether (ca 800 ml) affording N-[(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-10-yl)methyl]-5-hydroxyvaleramide, m.p. 96° - 98° C, γ maxCHCl3 3630, 3445, 3350, 1663 cm-1.

Workup

  1. temperatureThe mixture is heated for 2 hr
  2. customat 150° C
  3. customThe ethanol is removed under reduced pressure
  4. extractionthe residual mixture extracted with chloroform
  5. washThe chloroform solution is washed with water
  6. customdried
  7. customThe residue is crystallized from benzene (750 ml) -ether (ca 800 ml)

Sources & evidence

ORD record
ord-c03a376750db4fe0ad8b98502bfa3452
Source dataset
uspto-grants-1976_10
Patent number
US03985751

Reaction notes

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