Tetrahydrofuran → HCID 15676317, compound

Ten grams (0.102 mole) of 3,3-dimethyl-3-methoxy-1-propyne, produced according to the method described in Zh. Org. Khim., 2(11), 1969-1973 (1966), was dissolved in 100 ml of anhydrous tetrahydrofuran, and the resulting solution was cooled to -40° C. or less in a dry ice-acetone bath. Under a stream of a nitrogen gas, 68 ml of 1.5M hexane solution of n-butyllithium was added dropwise at -40° C. or less with stirring. After aging the reaction solution at -50° C. for 30 minutes, 7.53 g (0.102 mole) of 2-fluoroacrolein was added dropwise at -50° C. or less. After the reaction mixture was allowed to stand overnight at room temperature, it was poured into 200 ml of ice water and extracted with two 100-ml portions of ethyl acetate. The organic layers were combined, washed once with 100 ml of a saturated aqueous sodium chloride solution and concentrated under reduced pressure. The residue was distilled under reduced pressure to obtain 3 g of 2-fluoro-3-hydroxy-6,6-dimethyl-6-methoxyhex-1-ene-4-yne.

1. temperaturethe resulting solution was cooled to -40° C. or less in a dry ice-acetone bath
2. customat -50° C.
3. customfor 30 minutes
4. extractionextracted with two 100-ml portions of ethyl acetate
5. washwashed once with 100 ml of a saturated aqueous sodium chloride solution
6. concentrationconcentrated under reduced pressure
7. distillationThe residue was distilled under reduced pressure

ORD record

ord-424ae609d5e648b499d395ef3244af9a

Source dataset

uspto-grants-1991_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05028714