Sodium Hydroxide → HCID 19779518, compound

HRID 847142Notes

Reaction equation

HRID 847142 reaction equation
ClC1C=C(C=CC=1)C(OO)=[O:6].[Cl:12][CH2:13][CH2:14][CH2:15][S:16][C:17]1[CH:22]=[CH:21][C:20]([N+:23]([O-:25])=[O:24])=[CH:19][CH:18]=1.C(=O)=O.CC(C)=O.[OH-].[Na+]>C(Cl)Cl>[Cl:12][CH2:13][CH2:14][CH2:15][S:16]([C:17]1[CH:22]=[CH:21][C:20]([N+:23]([O-:25])=[O:24])=[CH:19][CH:18]=1)=[O:6]

Participants

6

Procedure

A solution of m-chloroperoxybenzoic acid (80%, 16.6 g, 86.3 mmol) in methylene chloride (100 mL) was added dropwise to a solution of 1-[(3-chloropropyl)thio]-4-nitrobenzene (20.0 g, 86.3 mmol) in methylene chloride (200 mL) maintained at -78° C. (dry ice/acetone bath). After 2 h the reaction was allowed to warm to ambient temperature (~1 h) and 200 mL of 10% aqueous sodium hydroxide was added. The layers were allowed to separate and the aqueous layer was extracted (100 mL) with methylene chloride. The combined organic extracts were washed (water, 100 mL), dried (MgSO4) and concentrated in vacuo. A 1.0 g sample of the residue (21.2 g) was chromatographed (Chromatatron, SiO2, 4000μ, 99/1, methylene chloride:methanol) to give 0.89 g (88%) of white solid, mp 72.5°-74.5° C.

Workup

  1. additionwas added
  2. customto separate
  3. extractionthe aqueous layer was extracted (100 mL) with methylene chloride
  4. washThe combined organic extracts were washed (water, 100 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customA 1.0 g sample of the residue (21.2 g) was chromatographed (Chromatatron, SiO2, 4000μ, 99/1, methylene chloride:methanol)

Sources & evidence

ORD record
ord-e11f2cb5049e42109d7a624b12f1de75
Source dataset
uspto-grants-1992_08
Patent number
US05140026

Reaction notes

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