4-(Trifluoromethyl)benzaldehyde → HCID 57991912, compound

To a mixture of (R)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine (5.2 mL, 29 mmol) (commercially available from 3B Scientific Corporation Product List (Order Number 3B3-054672)) and THF (50 mL) at −78° C. was added n-butyllithium (2.5 M solution in hexane, 12 mL, 31 mmol). The mixture was stirred for 15 minutes. The colorless solution turned light brown. A solution of 4-(trifluoromethyl)benzaldehyde (5.1 mL, 38 mmol) (commercially available from 3B Scientific Corporation Product List (Order Number 3B4-3644)) in THF (50 mL) was added dropwise through a dropping funnel at −78° C. The mixture was stirred for 1 hour. The reaction mixture was diluted with EtOAc and washed with a mixed solution of aqueous Na2HPO4 and KH2PO4 solution (pH=8). The aqueous layer was extracted with EtOAc three times. The combined organic layers were washed with water and brine, dried over Na2SO4, and concentrated in vacuo. The crude residue was separated into two isomers by silica gel chromatography: 0-2%-10% CH3CN—CH2Cl2. The product was obtained as light yellow oil (2.3 g, 22%). LCMS (API-ES) m/z: 359 (M+H+).

1. stirringThe mixture was stirred for 1 hour
2. washwashed with a mixed solution of aqueous Na2HPO4 and KH2PO4 solution (pH=8)
3. extractionThe aqueous layer was extracted with EtOAc three times
4. washThe combined organic layers were washed with water and brine
5. dry with materialdried over Na2SO4
6. concentrationconcentrated in vacuo
7. customThe crude residue was separated into two isomers by silica gel chromatography

ORD record

ord-495b5d30d24e4a95867ca5b1f67dfea8

Source dataset

uspto-grants-2011_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07919504B2