Hexane → HCID 15676316, compound

Ten grams (0.122 mole) of 3,3-dimethyl-1-butyne 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, 81.13 ml of a 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, 9.01 g (0.122 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 resulting oily product was distilled under reduced pressure to obtain 11 g of 2-fluoro-3-hydroxy-6,6-dimethylhept-1 -ene-4-yne (bp20, 86° C.).

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 resulting oily product was distilled under reduced pressure

ORD record

ord-f16f8e6359d24bf3a4919db7222e2bd9

Source dataset

uspto-grants-1990_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04980345