1-Butanol → HCID 2724555, compound

HRID 1656669Notes

Reaction equation

HRID 1656669 reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH:5]=[O:6].[CH2:7](O)[CH2:8][CH2:9][CH3:10]>>[CH2:7]([O:6][CH:5]1[CH2:4][CH2:3][CH2:2][O:1]1)[CH2:8][CH2:9][CH3:10]

Participants

3

Conditions

Temperature
22 °C

Procedure

Aqueous 4-hydroxybutanal (502 g of 10.2 wt. % solution, 0.58 mol, 1.0 eq.), n-butanol (34.6 g, 0.47 mol, 0.80 eq.), hexanes (500 mL), and "Amberlyst-15" resin (product of Rohm and Haas Company, 2.3 g) are charged to a 2-L glass reaction vessel equipped with a magnetic stir bar. The two-phase mixture is stirred at ambient temperature (22° C.) for 17 h. The two liquid phases are separated from the ion-exchange resin. The hexane layer, which is separated from the aqueous phase and analyzed by gas chromatography (GC), contains 14.8 wt. % of 2-n-butoxytetrahydrofuran (59.4 g, 88.5% yield). Product identity is confirmed by infrared, 1H NMR, and 13C NMR spectroscopies. The aqueous phase contains 4.2% unreacted 4-hydroxybutanal.

Workup

  1. customequipped with a magnetic stir bar
  2. customThe two liquid phases are separated from the ion-exchange resin
  3. customThe hexane layer, which is separated from the aqueous phase

Sources & evidence

ORD record
ord-83809446ea4a4f74a6597619401b2e81
Source dataset
uspto-grants-1993_10
Patent number
US05254702

Reaction notes

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