2-Pentynoic acid, 4-hydroxy-, ethyl ester → HCID 9989379, compound

Temperature

-70 °C

NaAlH2[O(CH2)2OMe]2 (68.6% m/m, 82.2 g, 0.270 mol) is dissolved in THF (750 ml) and cooled to −70° C. 20 (rac-Ethyl 4-hydroxypent-2-inoate) (crude, HPLC: ˜90 area %, 21.33 g, 0.135 mol) in THF (500 ml) is added dropwise over 1.25 h at ≦−65°. After stirring for 2 hours at ≦−68° C. the reaction mixture is quenched with 2 M HCl (540 ml). Then water (250 ml) is added and the mixture is extracted with tBuOMe (1.5 and 1 l). The organic phases are washed with saturated NaHCO3 (250 ml) and brine (2×100 ml) successively. The combined organic phases are dried with Na2SO4 and evaporated under reduced pressure at 40° C. The residue is purified by flash chromatography (AcOEt:heptane fraction 20:80 to 40:60) and yields 21 (rac-Ethyl (2E)-4-hydroxypent-2-enoate) (15.56 g, 80%) as a yellow oil.

1. customis quenched with 2 M HCl (540 ml)
2. additionThen water (250 ml) is added
3. extractionthe mixture is extracted with tBuOMe (1.5 and 1 l)
4. washThe organic phases are washed with saturated NaHCO3 (250 ml) and brine (2×100 ml) successively
5. dry with materialThe combined organic phases are dried with Na2SO4
6. customevaporated under reduced pressure at 40° C
7. customThe residue is purified by flash chromatography (AcOEt:heptane fraction 20:80 to 40:60)

ORD record

ord-8c166a7375f04fe19ac143bfeb725d0e

Source dataset

uspto-grants-2012_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08288566B2