Water → 3-(4-Chlorophenyl)-3-methylbutyraldehyde

Under a nitrogen atmosphere, a stirred solution of 21.6 grams (0.10 mole) of 4-chlorophenylmagnesium bromide (1M in diethyl ether) in 100 mL of tetrahydrofuran is cooled to -15° C., and 0.7 grams (catalyst) of copper(I) bromide is added in one portion. Upon completion of addition, 9.7 mL (0.10 mole) of 3-methyl-2-butenal is added dropwise during a 1.5 hour period, while maintaining the reaction mixture temperature below -10° C. Upon completion of addition, the reaction mixture is allowed to warm to ambient temperature, where it is stirred for about 18 hours. The reaction mixture is then poured into 300 mL of water and extracted with two 200 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel, using 50% petroleum ether in methylene chloride as the eluant. The appropriate product-containing fractions are combined and concentrated under reduced pressure, yielding 7.6 grams of 3-(4-chlorophenyl)-3-methylbutyraldehyde. The NMR spectrum is consistent with the proposed structure. The reaction is repeated.

1. additionis added dropwise during a 1.5 hour period
2. temperaturewhile maintaining the reaction mixture temperature below -10° C
3. additionUpon completion of addition
4. extractionextracted with two 200 mL portions of diethyl ether
5. dry with materialThe combined extracts are dried with magnesium sulfate
6. filtrationfiltered
7. concentrationThe filtrate is concentrated under reduced pressure to a residue
8. additionThe appropriate product-containing fractions
9. concentrationconcentrated under reduced pressure

ORDレコード

ord-9c9e56189438421baff4ea399f4c1945

出典データセット

uspto-grants-1997_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05622954