Hydrochloric Acid → 2,2-Dimethylpentanoic acid

A 240 ml (285 mmol) portion of a solution of t-butyllithium in pentane (1.18M) was added dropwise to a solution of 42 ml (290 mmol) of diisopropylamine in 300 ml of dry tetrahydrofuran while it was stirred with -5° bath cooling under argon. A 12.7 ml (135 mmol) portion of 2-methylpropionic acid in 15 ml of dry tetrahydrofuran was then added dropwise to the reaction mixture. A 14.3 ml (140 mmol) portion of n-propyliodide was then added dropwise to the reaction mixture as stirring was continued with ice bath cooling. The resultant mixture was stirred two hours without cooling and then acidified by the slow addition of 10% hydrochloric acid. The resultant mixture was extracted several times with ether and the combined extracts were washed with brine, dried (Na2SO4) and evaporated in vacuo to yield 16.3 g of 2,2-dimethylpentanoic acid, having the following spectral characteristics: nmr (CDCl3) δ 0.94 (3H, t, J=8.5 Hz), 1.20 (6H, s), 1.2-1.8 (4H, m) and 11.3 ppm (1H, broad s); ir (CHCl3) 860, 945, 1185, 1240, 1290, 1310, 1370, 1410, 1480, 1700 and 2400-3400 cm-1 (broad).

1. temperaturecooling under argon
2. stirringas stirring
3. customwas continued with ice bath
4. temperaturecooling
5. temperaturewithout cooling
6. extractionThe resultant mixture was extracted several times with ether
7. washthe combined extracts were washed with brine
8. dry with materialdried (Na2SO4)
9. customevaporated in vacuo

ORD record

ord-30aefb1ccde8424baecf12e601fce89f

Source dataset

uspto-grants-1988_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04742080