Trifluoroacetic acid → (R)-2-hexyl-6-iodo-1,2,3,4-tetrahydronaphthalene

To a stirred solution of (R)-2-hexyl-6-iodo-3,4-dihydronaphthalen-1(2H)-one (I-8C, 21.6 g, 60.6 mmol) in dichloromethane (10 mL) and 100% EtOH (100 mL) was added sodium borohydride (4.59 g, 121 mmol) portionwise. The mixture was stirred at room temperature for 2 h before being quenched by adding acetone slowly (cooled with water bath). The mixture was concentrated under reduced pressure. The residue was mixed with saturated aqueous ammonium chloride solution (100 mL) and water (50 mL) and extracted with ethyl acetate (100 mL, 2×50 mL). The combined ethyl acetate extracts were dried over anhydrous sodium sulfate and concentrated under reduced pressure to give an oil. The oil was dissolved in triethylsilane (70 mL, 438 mmol). TFA (100 mL, 1298 mmol) was added with vigorous stirring. The mixture was stirred at room temperature under nitrogen for 2.5 h. After water (150 mL) was added, the mixture was extracted with hexanes (100 mL, 2×50 mL). The combined extracts were washed with water (50 mL) and then saturated aqueous sodium bicarbonate solution (50 mL), dried over anhydrous sodium sulfate, and concentrated to give a yellow liquid. Flash chromatography purification (330 g silica gel column, gradient elution from 0 to 12% EtOAc in hexanes) afforded (R)-2-hexyl-6-iodo-1,2,3,4-tetrahydronaphthalene (18.4 g, 53.8 mmol) as a colorless liquid. 1H NMR (400 MHz, chloroform-d) δ 7.41 (s, 1H), 7.38 (dd, J=7.9, 1.8 Hz, 1H), 6.79 (d, J=8.1 Hz, 1H), 2.82-2.71 (m, 3H), 2.31 (dd, J=16.5, 10.6 Hz, 1H), 1.93-1.85 (m, 1H), 1.72-1.60 (m, 1H), 1.41-1.24 (m, 11H), 0.92-0.85 (m, 3H). Chiral SFC separation (CHIRALPAK® AS-H 25×3.0 cm, 5 nm, CO2/MeOH=95/5, 180 mL/min, 230 nm) gave (R)-2-hexyl-6-iodo-1,2,3,4-tetrahydronaphthalene (11.8 g, PK2) and its (S)-isomer (1.4 g, PK1) as liquids.

1. custombefore being quenched
2. additionby adding
3. temperatureacetone slowly (cooled with water bath)
4. concentrationThe mixture was concentrated under reduced pressure
5. additionThe residue was mixed with saturated aqueous ammonium chloride solution (100 mL) and water (50 mL)
6. extractionextracted with ethyl acetate (100 mL, 2×50 mL)
7. dry with materialThe combined ethyl acetate extracts were dried over anhydrous sodium sulfate
8. concentrationconcentrated under reduced pressure
9. customto give an oil
10. stirringThe mixture was stirred at room temperature under nitrogen for 2.5 h
11. extractionthe mixture was extracted with hexanes (100 mL, 2×50 mL)
12. washThe combined extracts were washed with water (50 mL)
13. dry with materialsaturated aqueous sodium bicarbonate solution (50 mL), dried over anhydrous sodium sulfate
14. concentrationconcentrated
15. customto give a yellow liquid
16. customFlash chromatography purification (330 g silica gel column, gradient elution from 0 to 12% EtOAc in hexanes)

ORD record

ord-a1ec03f3cbab47d9967e2180081931a2

Source dataset

uspto-grants-2015_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09115054B2