Hydrochloric Acid → HCID 22644705, compound

HRID 2414542Notes

Reaction equation

HRID 2414542 reaction equation
[CH2:1]([OH:5])[C:2]#[C:3][CH3:4].[H-].[Na+].F[C:9]1[CH:14]=[CH:13][C:12]([S:15]([N:18]([CH3:26])[CH:19]([CH:23]([CH3:25])[CH3:24])[C:20]([OH:22])=[O:21])(=[O:17])=[O:16])=[CH:11][CH:10]=1.Cl>CN(C=O)C.O>[CH2:1]([O:5][C:9]1[CH:14]=[CH:13][C:12]([S:15]([N:18]([CH3:26])[CH:19]([CH:23]([CH3:24])[CH3:25])[C:20]([OH:22])=[O:21])(=[O:17])=[O:16])=[CH:11][CH:10]=1)[C:2]#[C:3][CH3:4]

Participants

7

Procedure

To a solution of 3.17 mL (0.042 mol) of 2-butyn-1-ol in 60 ml of DMF at room temperature was added 1.70 g (0.040 mol) 60% sodium hydride. The resulting mixture was stirred for 0.5 h and then a solution of 2.45 g (8.478 mmol) the product of Example 11 dissolved in 20 mL of DMF was added to the reaction. The reaction mixture was then heated to reflux for 24 h, cooled to room temperature and then acidified to pH 2 with 10% HCl solution. After stirring for 1 h the resulting mixture was diluted with water and extracted with ethyl acetate. The combined organics were then dried over MgSO4, filtered and concentrated in vacuo. The, residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:2) to provide 1.67 g (58%) of the desired carboxylic acid product as a white solid identical to the product of Example 8.

Workup

  1. additionwas added to the reaction
  2. temperatureThe reaction mixture was then heated
  3. temperatureto reflux for 24 h
  4. stirringAfter stirring for 1 h the resulting mixture
  5. extractionextracted with ethyl acetate
  6. dry with materialThe combined organics were then dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe, residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:2)

Sources & evidence

ORD record
ord-ce6dcbd13c4a4fb48be0559cf87127a3
Source dataset
uspto-grants-2004_11
Patent number
US06812227B2

Reaction notes

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