Tetrahydrofuran → Cyclooctylthiourea

HRID 1158066Notes

Reaction equation

HRID 1158066 reaction equation
C([NH:9][C:10]([NH:12][CH:13]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)=[S:11])(=O)C1C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+].C1COCC1>CO.O>[CH:13]1([NH:12][C:10]([NH2:9])=[S:11])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

Participants

6

Reactant 3

HCID 8028TetrahydrofuranHCID 11430Potassium CarbonateHCID 589299211-Benzoyl-3-cyclooctylthiourea

Product 1

HCID 14677887Cyclooctylthiourea

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Procedure

A mixture of 1-benzoyl-3-cyclooctylthiourea (14.3 g, 49.1 mmol) and potassium carbonate (34.6 g, 250 mmol) in methanol (200 mL), water (100 mL), and THF (100 mL) was stirred at ambient temperature overnight. The low boiling solvents were removed in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was washed with brine, and concentrated in vacuo. The title compound was obtained as a white solid after flash column chromatography (0 to 100% of ethyl acetate in hexanes). MS m/z: 187.1 (M+H)+.

Workup

  1. customThe low boiling solvents were removed in vacuo
  2. customthe residue was partitioned between EtOAc and water
  3. washThe organic portion was washed with brine
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-eb4b6eedb6ba4af19d27dc2e05216f64
Source dataset
uspto-grants-2010_10
Patent number
US07807700B2

Reaction notes

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