Sodium Bicarbonate → HCID 18457684, compound

HRID 853771Notes

Reaction equation

HRID 853771 reaction equation
[CH3:1][CH:2]([CH3:4])O.[N:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[Li]CCCC.C([O-])(O)=O.[Na+]>C1COCC1>[CH2:1]=[CH:2][CH3:4].[N:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

Participants

5

Conditions

Temperature
-78 °C

Procedure

To a solution of O-protected pyridine dimethylcarbinol (3.0 g, 10.6 mmol) in THF (50 mL) at −78° C. was added n-BuLi 2.5 N in hexanes (4.7 ml, 11.7 mmol) followed, 1 min later, by phenylthionochloroformate (2.76 g, 16.0 mmol). The reaction was stirred at −78° C. for 40 min, then allowed to warm to RT and stirred 4 h. The final mixture was treated with saturated NaHCO3, extracted with DCM and AcOEt and the combined organic layers were dried over Na2SO4 and concentrated. Purification of the residue by flash chromatography over silica gel (eluting with hexane to DCM) afforded 1.5 g of O-protected pyridine propene as well as 1.8 g of starting O-protected pyridine dimethylcarbinol.

Workup

  1. temperatureto warm to RT
  2. stirringstirred 4 h
  3. extractionextracted with DCM and AcOEt
  4. dry with materialthe combined organic layers were dried over Na2SO4
  5. concentrationconcentrated
  6. customPurification of the residue by flash chromatography over silica gel (eluting with hexane to DCM)

Sources & evidence

ORD record
ord-a4180cc606ee437ea37ae1a95ecc0216
Source dataset
uspto-grants-2007_08
Patent number
US07256186B2

Reaction notes

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