tert-Butanol → (R)-(-)-1,2,3,4-Tetrahydro-1-naphthol

Temperature

60 °C

General procedure for hydrogenation: Hydrogenation of 28 illustrates the typical reaction procedure: To a mixture of 1-tetralone, 28, (10.0 g, 66.4 mmol) and RuCl2[(2R,2′R,3S,3′S)-MeO-BIBOP](amqui), 27, (1.0 mg, 0.001 mmol, 0.002 mol %) was added isopropanol (40 mL) and a 1 M solution of t-BuOK in tert-butanol (1.33 mL, 1.33 mmol, 0.02 equiv). The autoclave reactor was first purged with nitrogen, then with hydrogen, and then the reaction mixture was stirred at 60° C. under 400 psi of hydrogen for 20 h. After venting the hydrogen gas, the solvent was removed under reduced pressure. The residue was purified by silica-gel column chromatography with ethyl acetate/hexane (0-50%) as eluent to give (R)-1,2,3,4-tetrahydro-1-naphthol, 29, (colorless oil, 9.6 g, 98% yield, 96:4 er). The er of 1,2,3,4-tetrahydro-1-naphthol was determined by HPLC analysis: column, Chiralcel OJ-3, 4.6×150 mm; eluent, heptane/isopropanol (95:5); flow rate, 1 mL/min; column temperature, 25° C.; retention time (tR) of (R)-1,2,3,4-tetrahydro-1-naphthol, 7.45 min (95.8%); tR of (S)-1,2,3,4-tetrahydro-1-naphthol, 5.75 min (4.2%). [α]D=−31.2 (c=2.0, MeOH).

1. customthe typical reaction procedure
2. customThe autoclave reactor was first purged with nitrogen
3. customthe solvent was removed under reduced pressure
4. customThe residue was purified by silica-gel column chromatography with ethyl acetate/hexane (0-50%) as eluent

ORD record

ord-d26dae10e3194b47bf8146ae326b1c45

Source dataset

uspto-grants-2015_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09029540B2