HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365419Generated: November 2, 2026
Aluminium lithium hydride → HCID 67969245, compound
https://huagongshe.com/reaction/2365419
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 6-bromo-1-methyl-2-(2-nitrovinyl)-1H-indole | HCID 67969201 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67969245 | HCID 67969245 | 42% |
Reaction Steps
To a solution of 6-bromo-1-methyl-2-(2-nitrovinyl)-1H-indole (871 mg, 3.10 mmol) in THF (60.0 mL) at 0° C. was added LiAlH4 (2.0 M in THF, 6.20 mL, 12.4 mmol) dropwise. The reaction mixture was allowed to warm to room temperature over 5 h and then quenched with water and 10% aqueous NaOH (20 mL) at 0° C. to form a precipitate which was filtered through filter paper. The filtrate was extracted with EtOAc. The extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by flash chromatography (silica gel, CH2Cl2/(80:18:2 CH2Cl2/MeOH/NH4OH), 90:10 to 20:80) gave the title compound (329 mg, 42%) as a brown oil: 1H NMR (500 MHz, CDCl3) δ 7.42 (s, 1H), 7.38 (d, J=8.5 Hz, 1H), 7.17 (dd, J=8.5, 2.0 Hz, 1H), 6.27 (d, J=1.0 Hz, 1H), 3.65 (s, 3H), 3.08-3.55 (m, 2H), 2.92-2.87 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697700B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-02b489009e8d4bc8a63d0105ba3b0f2f |
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| Source note | uspto-grants-2014_04 |
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