Hydrochloric Acid → 4-(Trimethylsilyl)but-3-yn-2-ol

Temperature

0 °C

To a solution of ii (10.0 g, 0.14 mol) in ether (200 mL) was added ethylmagnesium bromide (105 mL, 3 M in THF, 0.32 mol) dropwise at 0° C. The resulting solution was refluxed for 1.5 h. After the reaction solution was cooled to 0° C., trimethylsilyl chloride (40 mL, 0.32 mol) was added. The solution was warmed to room temperature and stirred overnight. Hydrochloric acid (100 mL, 10%) was added at 0° C. After 20 min, the two layers were separated. The aqueous layer was extracted with ether (2×50 mL). The combined organic solutions were dried over anhydrous magnesium sulfate, filtered and concentrated. Distillation of the residue gave 19.9 g (98%) ii-a as a colorless liquid: bp 80.5°-83.5° C. /17.5 mm Hg; IR (neat) 3337, 2175, 1452, 1251, 1119, 1048, and 946 cm-1 ; 1NMR (CDCl3, 300 MHz) δ4.42 (q, J=6.6 Hz, 1H, CHOH), 3.12 (br s, 1H, OH), 1,16 (d, J=6.6 Hz, 3H, CHCH3), and 0.08 (s, 9H, SiCH3); 13C NMR (CDCl3, 75.5 MHz) δ108.12, 88.19, 58.61, 24. 05, and 0.01.

1. temperatureThe resulting solution was refluxed for 1.5 h
2. temperatureThe solution was warmed to room temperature
3. waitAfter 20 min
4. customthe two layers were separated
5. extractionThe aqueous layer was extracted with ether (2×50 mL)
6. dry with materialThe combined organic solutions were dried over anhydrous magnesium sulfate
7. filtrationfiltered
8. concentrationconcentrated
9. distillationDistillation of the residue
10. customgave 19.9 g (98%) ii-a as a colorless liquid

ORD record

ord-69598726c43748349dfdd5e8d27f5ff8

Source dataset

uspto-grants-1996_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05587491