Sodium Chloride → HCID 21187855, compound

HRID 356926Notes

Reaction equation

HRID 356926 reaction equation
[CH3:1][S-:2].[Na+].[CH:4]1([O:9][C:10]2[CH:11]=[C:12]([CH:21]=[CH:22][C:23]=2[N+]([O-])=O)[C:13]([O:15][CH:16]2[CH2:20][CH2:19][CH2:18][CH2:17]2)=[O:14])[CH2:8][CH2:7][CH2:6][CH2:5]1.[Cl-].[Na+]>CN1CCN(C)C1=O.O>[CH:4]1([O:9][C:10]2[CH:11]=[C:12]([CH:21]=[CH:22][C:23]=2[S:2][CH3:1])[C:13]([O:15][CH:16]2[CH2:20][CH2:19][CH2:18][CH2:17]2)=[O:14])[CH2:8][CH2:7][CH2:6][CH2:5]1

Participants

6

Reactant 3

HCID 5234Sodium ChlorideHCID 4378561Sodium methanethiolateHCID 21187914Cyclopentyl 3-cyclopentyloxy-4-nitrobenzoate

Product 1

HCID 21187855HCID 21187855, compoundYield 81.1%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 66611,3-Dimethyl-2-imidazolidinoneSolvent

Procedure

Sodium thiomethoxide (0.177 g, 2.5 mmol) is added portionwise to a stirred solution of cyclopentyl 3-cyclopentyloxy-4-nitrobenzoate (0.64 g, 2 mmol) in N,N'-dimethylimidazolidinone (10 mL) at ambient temperature under an atmosphere of nitrogen and stirring continued for 4 hours. The mixture is then diluted with water (100 mL) containing sodium chloride (15 g) and extracted with ethyl acetate (2×50 mL). The combined extract is washed with saturated brine (1×100 mL) and then dried over magnesium sulfate and evaporated under reduced pressure to give cyclopentyl 3-cyclopentyloxy-4-(methylthio)benzoate (0.52 g, 81%) as a brown viscous oil which is used without further purification.

Workup

  1. extractionextracted with ethyl acetate (2×50 mL)
  2. extractionThe combined extract
  3. washis washed with saturated brine (1×100 mL)
  4. dry with materialdried over magnesium sulfate
  5. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-41b6e827c6674f6b870b679e0211a228
Source dataset
uspto-grants-1998_11
Patent number
US05840724

Reaction notes

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