HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → (2R)-8-Amino-1,2,3,4-tetrahydro-2-naphthalenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 91257777 | HCID 91257777 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R)-8-Amino-1,2,3,4-tetrahydro-2-naphthalenol | HCID 57936087 | 82% |
Reaction Steps
A mixture of Example 24D (3.05 g, 9.80 mmol) in tetrahydrofuran (40 mL) and lithium hydroxide (1 M aq, 30 mL, 30.0 mmol) was stirred vigorously at ambient temperature. After 1.5 hours the reaction mixture was partitioned between 100 mL ethyl acetate:H2O (1:1). The separated organic phase was washed with aq saturated NaHCO3 and brine, dried over Na2SO4, and filtered. The solvent was removed at the rotary evaporator to yield 1.31 g (82% yield) of the title compound as a tan solid. 1H NMR (300 MHz, DMSO-d6) δ 6.76 (t, 1H), 6.41 (d, 1H), 6.28 (d, 1H), 4.74, (d, 1H), 4.65 (bs, 2H), 3.90 (m, 1H), 2.52-2.79 (m, 3H), 2.16 (m, 1H), 1.83 (m, 1H), 1.55 (m, 1H). MS (DCI+) m/z 164 (M+H)+, 181 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998993B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-6a75acd2fc6a4656b9829fd1d85c597f |
| Source note | uspto-grants-2011_08 |