4-Hydroxybenzaldehyde → 4-(2,2,2-Trifluoroethoxy)benzaldehyde

Potassium hydroxide pellets (85%, 13.2 g, 0.2 mol) are added to 4-hydroxybenzaldehyde (24.4 g, 0.2 mol) and 18-crown-6 (2.6 g, 5% mol) in diglyme (150 mL). The red reaction mixture is stirred for 16 hours at room temperature and then a solution of 2,2,2-trifluoroethyl-p-toluenesulfonate (50.8 g, 0.2 mol) in diglyme (100 mL) is added over 30 minutes, after which the mixture is allowed to stir at room temperature for 45 minutes. The resulting suspension is then heated at reflux for 24 hours. The mixture is cooled to 10° C. and poured into ice water (1300 mL). The organic materials are extracted with ether (4×200 mL), and the extracts washed with 5% sodium hydroxide (2×100 mL), water (2×100 mL) and saturated sodium chloride (1×100 mL), and dried over MgSO4. Evaporation of the ether gives an amber oil which is purified by high performance liquid chromatography using silica gel on a Waters 500 unit and 50:50 hexane and methylene chloride as eluant to give 12.3 g of the title product with Rf 0.25. Anal. Calcd for C9H7F3O2 (204.15) C, 52.94; H, 3.43. Found C, 52.04; H, 3.59.

1. customThe red reaction mixture
2. stirringto stir at room temperature for 45 minutes
3. temperatureThe resulting suspension is then heated
4. temperatureat reflux for 24 hours
5. temperatureThe mixture is cooled to 10° C.
6. extractionThe organic materials are extracted with ether (4×200 mL)
7. washthe extracts washed with 5% sodium hydroxide (2×100 mL), water (2×100 mL) and saturated sodium chloride (1×100 mL)
8. dry with materialdried over MgSO4
9. customEvaporation of the ether
10. customgives an amber oil which
11. customis purified by high performance liquid chromatography

ORD 기록

ord-6770dc6d28744c09bf7f645291d24b0a

출처 데이터셋

uspto-grants-1986_03

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US04575560