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Sodium borohydride → HCID 12096237, compound

HRID 2120095
Notes
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Reaction equation

HRID 2120095 reaction equation
[Br:1][C:2]1[C:10]2[S:9](=[O:12])(=[O:11])[N:8](C(C)(C)C)[CH:7](O)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>C(O)=O>[Br:1][C:2]1[C:10]2[S:9](=[O:12])(=[O:11])[NH:8][CH2:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 12046097HCID 12046097, compound

Product 1

HCID 12096237HCID 12096237, compoundYield 60%

Reagents, catalysts & solvents 1

HCID 284Formic AcidSolvent

Procedure

7-bromo-2-(1,1-dimethylethyl)-2,3-dihydro-1,2-benzisothiazol-3-ol 1,1-dioxide (1.4 g, 4.4 mmol) was treated with formic acid (10 mL). The reaction was stirred at ambient temperature over 18 h, concentrated in vacuo and dissolved in methanol (10 mL). The mixture was cooled to 0° C. and treated with sodium borohydride (0.17 g, 4.4 mmol) in small portions over 20 min. The cooling bath was removed and the resulting reaction mixture stirred at ambient temperature over 18 h. The work-up consisted of slowly quenching the reaction mixture with ice, dilution with water and extraction with ethyl acetate. Drying over sodium sulfate and concentrating under reduced pressure provided the crude product that was purified by a plug of silica gel (ethyl acetate/hexane, 1:4) to afford the desired 7-bromo-2,3-dihydro-1,2-benzisothiazole 1,1-dioxide (0.6 g, 60% over 2 steps). 1H NMR (CD3OD): δ 4.40 (s, 2H), 7.53 (m, 2H), 7.70 (m, 1H).

Workup

  1. concentrationconcentrated in vacuo
  2. dissolutiondissolved in methanol (10 mL)
  3. temperatureThe mixture was cooled to 0° C.
  4. customThe cooling bath was removed
  5. customthe resulting reaction mixture
  6. stirringstirred at ambient temperature over 18 h
  7. customof slowly quenching the reaction mixture with ice, dilution
  8. extractionwith water and extraction with ethyl acetate
  9. dry with materialDrying over sodium sulfate
  10. concentrationconcentrating under reduced pressure
  11. customprovided the crude product that
  12. customwas purified by a plug of silica gel (ethyl acetate/hexane, 1:4)

Sources & evidence

ORD record
ord-f56605e438564dce8c22865dbdf3b224
Source dataset
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06689770B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes