Hexane → 4-Butylcyclopent-2-ene-1,4-diol

温度

-78 °C

30 ml of tetrahydrofuran was put in a reaction tube and cooled to -78° C., and n-butyllithium (as a 1.6M hexane solution; 13.8 ml, 22.08 mmmoles) was added dropwise. Then a solution of 4-hydroxy-2-cyclopentenone (987 mg; 10.1 mmoles) in 20 ml of tetrahydrofuran was added dropwise over about 20 minutes. The reaction mixture was washed with 8 ml of tetrahydrofuran. After 60 minutes, 40 ml of a saturated aqueous solution of ammonium chloride was added, and the mixture was vigorously shaken. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate (20 ml×6). The extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The residue was chromatographed on a silica gel column (Merck silica gel 30 g; hexane:ethyl acetate=4:1) to obtain 1.55 g (yield about 90%) of 4-butylcyclopent-2-ene-1,4-diol.

1. addition13.8 ml, 22.08 mmmoles) was added dropwise
2. washThe reaction mixture was washed with 8 ml of tetrahydrofuran
3. addition40 ml of a saturated aqueous solution of ammonium chloride was added
4. customThe organic layer was separated
5. extractionthe aqueous layer was extracted with ethyl acetate (20 ml×6)
6. dry with materialThe extracts were dried over anhydrous sodium sulfate
7. filtrationfiltered
8. concentrationconcentrated
9. customThe residue was chromatographed on a silica gel column (Merck silica gel 30 g; hexane:ethyl acetate=4:1)

ORDレコード

ord-17e7da63bfa94232850e1cf29b6d6971

出典データセット

uspto-grants-1987_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04711895