Methyl 4-methyl-3-hydroxyhept-6-enoate → 4-Methyl-3-hydroxyhept-6-enoic acid

Methyl 4-methyl-3-hydroxyhept-6-enoate (5.72 g, 33.2 mmol) was dissolved in a 2 N potassium hydroxide-methanol solution (50 mL), and the solution was stirred overnight at room temperature. From the reaction solution, the solvent was distilled off under reduced pressure. To the residue, a 1 N aqueous sodium hydroxide solution was then added, followed by extraction with diethyl ether. The aqueous layer was made acidic by the addition of concentrated hydrochloric acid under ice cooling, followed by extraction with diethyl ether again. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a yellow oil substance (2.21 g, 42%, mixture of diastereomers).

1. distillationFrom the reaction solution, the solvent was distilled off under reduced pressure
2. additionTo the residue, a 1 N aqueous sodium hydroxide solution was then added
3. extractionfollowed by extraction with diethyl ether
4. additionThe aqueous layer was made acidic by the addition of concentrated hydrochloric acid under ice cooling
5. extractionfollowed by extraction with diethyl ether again
6. washThe organic layer was washed with saturated saline
7. dry with materialdried over anhydrous magnesium sulfate
8. distillationThen, the solvent was distilled off under reduced pressure
9. customto obtain the compound of interest
10. additionas a yellow oil substance (2.21 g, 42%, mixture of diastereomers)

ORD record

ord-2e444d7b7b5149279028a212267098cd

Source dataset

uspto-grants-2011_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07947738B2