Pentanal → HCID 18956625, compound

A 200 mL round bottom flask equipped with a magnetic stirring bar was charged with a solution of 0.86 g. of 1-hydroxyamylphosphonic acid, 1.97 g. of 1,2-epoxydodecane and 51 g. of n-valeraldehyde. No new phosphorus compounds were detected by 31PNMR after stirring for two weeks at room temperature. After an additional week at room temperature, there was no apparent reaction between the 1-hydroxyamylphosphonic acid and 1,2-epoxydodecane as ascertained from the 31PNMR. The reaction mixture was then washed three times with 5% sodium bicarbonate solution. The extractate contained no phosphorus component evident in the 31PNMR. The extractate was washed once with distilled water, dried over anhydrous magnesium sulfate and stripped on a rotary evaporator to give a colorless oil weighing 10.1 g. A major high boiling component of this solution, as determined by gas chromatographic mass spectroscopy was 2-n-amyl-4-n-decyl-1,3-dioxolane. These results indicate that no apparent reaction of 1-hydroxyamylphosphonic acid with 1,2-epoxydodecane occurs under conditions where 1,2-epoxydodecane reacts with the n-valeraldehyde to form 2-n-butyl-4-n-decyl-1,3-dioxolane.

1. customA 200 mL round bottom flask equipped with a magnetic stirring bar
2. additionwas charged with a solution of 0.86 g
3. waitAfter an additional week at room temperature
4. washThe reaction mixture was then washed three times with 5% sodium bicarbonate solution
5. washThe extractate was washed once with distilled water
6. dry with materialdried over anhydrous magnesium sulfate
7. customstripped on a rotary evaporator
8. customto give a colorless oil

ORD record

ord-7ec4076f41024fa280ec5425b2c1cf2a

Source dataset

uspto-grants-1994_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05364950