Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 22121613 | HCID 22121613 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22121593 | HCID 22121593 | 80% |
Reaction Steps
A 250 mL two necked round bottom flask equipped with a magnetic stir bar and a reflux condenser was charged with 0.28 g (7.5 mmol) of lithium aluminum hydride (LAH) and 10 mL of dry THF. The apparatus was purged with argon and a solution of 5e (0.98 g; 2.5 mmol) in dry THF was transferred via cannula to the LAH suspension under argon. The mixture was refluxed under argon for 2 h. After cooling the flask to rt, ice cold water was added dropwise carefully. Upon observation of a white precipitate, conc. HCl was rapidly added, followed by more cold water. The aqueous layer was extracted with a mixture of hexanes/Et2 0 (3×50 mL). The organic extracts were combined together, washed with saturated NaHCO3 (2×50 mL), brine (1×50 mL), dried over MgSO4 and concentrated by rotary evaporation. The residual oil was chromatographed on silica gel using a mixture of hexanes/Et2O (60/1) and gave 0.61 g (2.0 mmol, 80% yield) of 5f as a colorless liquid. 1H NMR (300 MHz, CDCl3): δ 0.91 (6H, t, J=7 Hz, CH3), 1.36-1.57 (12H, m), 1.85 (1H, t, SH), 2.53 (4H, t, J=8 Hz, CH2Ar), 3.79 (4H, d, SCH2), 7.04 (2H, s, Ar--H). 13C NMR (75 MHz, CDCl3): δ 14.0, 22.5, 25.8, 30.9, 31.9, 32.2, 130.32, 130.38, 135.7 and 140.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153322 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-1b195395d4b6429ca2835462290835b3 |
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| Source note | uspto-grants-2000_11 |
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