1,4-Butanediol → HCID 23282403, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- additionwas added dropwise under ice cooling
- temperatureThe reaction mixture was slowly warmed
- extractionextracted twice with diethyl ether
- washwashed with water
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- 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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