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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637058Generated: November 5, 2026

1-Tetralone → 1,2,3,4-Tetrahydro-2-naphthalenol

https://huagongshe.com/reaction/1637058

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-TetraloneHCID 10724—
Reactant(1R, 2S)-2-tert-butyl-2-aminophenylethanolHCID 86754982—
SolventTetrahydrofuranHCID 8028—
Product1,2,3,4-Tetrahydro-2-naphthalenolHCID 10747915.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Borane methylsulfide complex (neat, ~10M, 0.44 mL, 4.4 mmol) was added to a solution of (1R, 2S)-2-tert-butyl-2-aminophenylethanol [Angew. Chem. Int. Ed. Engl. 26 1141 (1987)] (120 mg, 0.62 mmol) in THF (22 mL) at ambient temperature and stirred for 16 hrs. α-Tetralone (906 mg, 6.2 mmol) as a solution in THF (3 mL) was added to the preceding solution over a 1 hr, stirred for 15 min after addition was completed, cooled to 0° C., and quenched with methanol (20 mL). After stirring the quenched reaction for 18 hrs, the solvents were removed under vacuum, the residual oil was dissolved in methylene chloride (30 mL), washed with pH 4 phosphate buffer (30 mL), water (30 mL), treated with magnesium sulfate, and the solvent was removed under vacuum to give the (R) tetralol 841 mg (91% yield) 82% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06037505
Source datasetuspto-grants-2000_03
ORD IDord-579d8f36b8e64514b3178a7d52565126
Source noteuspto-grants-2000_03