Benzyl Alcohol → HCID 178427655, compound

HRID 1066744Notes

Reaction equation

HRID 1066744 reaction equation
[NH2:1][CH2:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([C:9]([OH:11])=[O:10])[CH2:5][CH2:4]1.[C:12]1([CH3:22])[CH:17]=[CH:16][C:15]([S:18]([OH:21])(=[O:20])=[O:19])=[CH:14][CH:13]=1.[CH2:23](O)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>C1(C)C=CC=CC=1>[C:12]1([CH3:22])[CH:13]=[CH:14][C:15]([S:18]([OH:21])(=[O:19])=[O:20])=[CH:16][CH:17]=1.[NH2:1][CH2:2][C@H:3]1[CH2:4][CH2:5][C@H:6]([C:9]([O:11][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[O:10])[CH2:7][CH2:8]1

Participants

5

Procedure

A mixture of 10.0 g (63.6 mmol) of trans-4-aminomethylcyclohexane-1-carboxylic acid, 25.1 g (132 mmol) of 4-toluenesulfonic acid, 50 mL (482 mmol) of benzyl alcohol, and 75 mL of toluene was heated to reflux under a N2 atmosphere using a Dean-Stark trap to collect water formed during the reaction. During reflux, all solids dissolved to leave a colorless solution. After 3 hours at reflux, the solution began to turn yellow. Heat was removed, and the flask allowed to cool to room temperature. The solids which separated out were collected and washed with diethyl ether. There was obtained 24.5 g (58.4 mmol, 92% yield) of product as a white solid.

Workup

  1. temperaturewas heated
  2. temperatureto reflux under a N2 atmosphere
  3. customto collect water
  4. customformed during the reaction
  5. temperatureDuring reflux
  6. dissolutionall solids dissolved
  7. customto leave a colorless solution
  8. temperatureAfter 3 hours at reflux
  9. temperatureHeat
  10. customwas removed
  11. customThe solids which separated out
  12. customwere collected
  13. washwashed with diethyl ether

Sources & evidence

ORD record
ord-af5941fcacc147faa19f139b08656783
Source dataset
uspto-grants-2001_06
Patent number
US06245743B1

Reaction notes

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