1,4-Butanediol → HCID 23282403, compound

HRID 369674Notes

Reaction equation

HRID 369674 reaction equation
[CH2:1]([OH:6])[CH2:2][CH2:3][CH2:4][OH:5].[H-].[Na+].[H][H].[Cl:11][C:12]([Cl:16])=[CH:13][CH2:14]Cl>O>[Cl:11][C:12]([Cl:16])=[CH:13][CH2:14][O:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:6]

Participants

6

Conditions

Temperature
60 °C

Procedure

In a reaction vessel containing 9.02 g of 1,4-butanediol was put 2.20 g of 60% sodium hydride (in oil), and the mixture was stirred until the evolution of hydrogen gas ceased, to which 7.28 g of 1,1,3-trichloro-1-propene was added dropwise under ice cooling. The reaction mixture was slowly warmed and stirred at 60° C. for 3 hours, which was then poured into water and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over magnesium sulfate and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 1.40 g of 4-(3,3-dichloro-2-propenyloxy)butanol (yield, 14%).

Workup

  1. additionwas added dropwise under ice cooling
  2. temperatureThe reaction mixture was slowly warmed
  3. extractionextracted twice with diethyl ether
  4. washwashed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated
  7. customto give a crude product

Sources & evidence

ORD record
ord-b384991259ff49689b8c5b50a4ef09cf
Source dataset
uspto-grants-2000_10
Patent number
US06140274

Reaction notes

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