Methane → 3-(Acetyloxy)-2,2-dimethylpropanoic acid

To a stirred solution of 4.0 grams (0.023 mole) of methyl 3-acetoxy-2,2-dimethylpropionate in 50 ml of carbon tetrachloride under an argon atmosphere was added slowly via a syringe 9.2 grams (0.046 mole) of iodotrimethylsilane. Upon completion of addition the reaction mixture was stirred at ambient temperature for 60 hours. The reaction mixture was then heated at 50° for 1.5 hours, and at 65° for 18 hours. Nuclear magnetic resonance spectroscopy indicated the reaction had not gone to completion. The reaction mixture was heated at 65° for six days, then poured into 100 ml water. The mixture was stirred for 20 minutes and the carbon tetrachloride layer separated. The water layer was extracted with three portions of 50 ml each of methylene chloride. The methylene chloride extracts and the carbon tetrachloride layer were combined. The combination was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give a semi-solid residue. The semi-solid was dissolved in hot ethyl acetate and treated with decolorizing charcoal. The mixture was filtered and the filtrate concentrated under reduced pressure to give a solid residue. The solid was recrystallized from hexane to give 1.5 grams of 3-acetoxy-2,2-dimethylpropionic acid; mp 56°-59°.

1. additionUpon completion of addition the reaction mixture
2. temperatureThe reaction mixture was then heated at 50° for 1.5 hours
3. waitat 65° for 18 hours
4. temperatureThe reaction mixture was heated at 65° for six days
5. stirringThe mixture was stirred for 20 minutes
6. customthe carbon tetrachloride layer separated
7. extractionThe water layer was extracted with three portions of 50 ml each of methylene chloride
8. dry with materialThe combination was dried with magnesium sulfate
9. filtrationfiltered
10. concentrationThe filtrate was concentrated under reduced pressure
11. customto give a semi-solid residue
12. filtrationThe mixture was filtered
13. concentrationthe filtrate concentrated under reduced pressure
14. customto give a solid residue
15. customThe solid was recrystallized from hexane

ORD record

ord-ec5b3f9f47594d71826b3149dae41972

Source dataset

uspto-grants-1983_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04405357