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Ethanol → 3-(4-Iodo-1H-pyrazol-1-yl)cyclobutanol

HRID 511275
Notes
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Reaction equation

HRID 511275 reaction equation
[I:1][C:2]1[CH:3]=[N:4][N:5]([CH:7]2[CH2:10][C:9](=[O:11])[CH2:8]2)[CH:6]=1.[BH4-].[Na+].C(O)C>>[I:1][C:2]1[CH:3]=[N:4][N:5]([CH:7]2[CH2:8][CH:9]([OH:11])[CH2:10]2)[CH:6]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 702EthanolHCID 4311764Sodium borohydrideHCID 672547783-(4-iodo-1H-pyrazol-1-yl)cyclobutan-1-one2×

Product 1

HCID 672540253-(4-Iodo-1H-pyrazol-1-yl)cyclobutanolYield 94.9%

Conditions

Temperature
0 °C

Procedure

3-(4-Iodo-pyrazol-1-yl)cyclobutanone (Compound 100D, 1.000 g, 3.816 mmol), sodium borohydride (145.8 mg, 3.854 mmol) and ethanol (22.28 mL, 381.6 mmol) were added to a round bottom flask and the reaction mixture was stirred at 0° C. for 3 h. Reaction mixture was concentrated in vacuo and washed with water extracting with DCM. The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo to afford 956 mg of the final compound as colorless oil. Compound was taken on to the next step without further purification. MS (ES+): m/z 264.86 (100) [MH+]; HPLC: tR=2.50 min (Polar—5 min, ZQ3).

Workup

  1. customReaction mixture
  2. concentrationwas concentrated in vacuo
  3. washwashed with water extracting with DCM
  4. dry with materialThe organic layer was dried over anhydrous Na2SO4
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-669eb04e50fd463a84a95853cab1bf27
Source dataset
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09096624B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes