2-Chloroethanol → 2-(Pyridin-3-yloxy)ethan-1-ol

HRID 1789723Notes

Reaction equation

HRID 1789723 reaction equation
[OH:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.Cl[CH2:9][CH2:10][OH:11].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[N:4]1[CH:5]=[CH:6][CH:7]=[C:2]([O:1][CH2:9][CH2:10][OH:11])[CH:3]=1

Participants

5

Conditions

Temperature
130 °C

Procedure

A mixture of 3-hydroxypyridine (2.00 g, 21 mmol), 2-chloroethanol (1.69 g, 21 mmol) and K2CO3(8.7, 63 mmol) in DMF (10 mL) was stirred at 130° C. for 3 h. After cooling, the black mixture was filtered through a short bed of alumina using acetone as eluent to afford a brown oil which was partitioned between water (30 mL) and CH2Cl2 (40 mL). The aqueous phase was extracted with CH2Cl2(3×40 mL), and the combined organic extracts were dried over MgSO4 and filtered. The filtrate was concentrated to give, 0.55 g (19%) of the title compound as a light brown oil. Anal. (C7H9NO2.0.2H2O)C, H, N.

Workup

  1. temperatureAfter cooling
  2. filtrationthe black mixture was filtered through a short bed of alumina
  3. customto afford a brown oil which
  4. customwas partitioned between water (30 mL) and CH2Cl2 (40 mL)
  5. extractionThe aqueous phase was extracted with CH2Cl2(3×40 mL)
  6. dry with materialthe combined organic extracts were dried over MgSO4
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated
  9. customto give

Sources & evidence

ORD record
ord-a562681c19a441419ac5e98241e7db05
Source dataset
uspto-grants-2006_07
Patent number
US07071180B2

Reaction notes

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