Potassium Sodium Tartrate → HCID 22613819, compound

Temperature

-78 °C

2-(3,4-Dichlorophenyl)-4-(tetrahydropyran-2-yloxy)butanenitrile (20.2 g) (see Preparation 26) was dissolved in anhydrous toluene (300 ml) and cooled to −78° C. under a nitrogen atmosphere. Diisobutylaluminium hydride (85.6 ml of a 1.0 M solution in toluene) was then added dropwise. The mixture was stirred at −78° C. for 1.5 hours and then allowed to warm slowly to −40° C. Water (100 ml) and saturated aqueous ammonium chloride solution (50 ml) were carefully added (exothermic reaction) and the mixture allowed to warm to 10° C. before further addition of water (100 ml) and saturated aqueous ammonium chloride solution (50 ml). A 10% w/w aqueous solution of Rochelle's salt (potassium sodium tartrate tetrahydrate) (400 ml) was added and the mixture extracted with diethyl ether. The organic phase was dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to give a crude product. This was chromatographed on silica gel eluting with 98:2, by volume, dichloromethane:methanol to give 2-(3,4-dichlorophenyl)-4-(tetrahydropyran-2-yloxy)butan-1-al (17.02 g) as a yellow oil and as a mixture of diastereomers.

1. temperatureto warm slowly to −40° C
2. custom(exothermic reaction)
3. extractionthe mixture extracted with diethyl ether
4. dry with materialThe organic phase was dried over anhydrous sodium sulphate
5. customthe solvent removed under reduced pressure
6. customto give a crude product
7. customThis was chromatographed on silica gel eluting with 98:2, by volume, dichloromethane

ORD record

ord-50d35e944cd74572b4cc293e6e0657bb

Source dataset

uspto-grants-2001_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06207678B1