HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923586Generated: October 31, 2026
Tetrahydrofuran → HCID 178444053, compound
https://huagongshe.com/reaction/923586
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 178444049 | HCID 178444049 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178444053 | HCID 178444053 | 46% |
Reaction Steps
To a stirred solution of 2-(4-(heptyloxy)benzyl)-1H-benzo[d]imidazole-5-carbonitrile INT-46 (1.22 g, 3.51 mmol) in THF (20 mL) at 0° C. was added diisobutylaluminum hydride (12.3 mL, 12.3 mmol, 1 M in toluene). After 2 h the reaction mixture was poured onto Rochelle's salt (7.91 g, 28.0 mmol) in water (100 mL) and EA (50 mL) and stirred for 1 h. The layers were split and the aqueous layer was further extracted with EA (2×30 mL). The combined organics were washed with brine (20 mL) dried over MgSO4 and evaporated. The crude material was purified by chromatography (EA/isohexanes) to afford 571 mg (46%) of 2-(4-(heptyloxy)benzyl)-1H-benzo[d]imidazole-5-carbaldehyde INT-47 as a brown oil. LCMS-ESI (m/z) calculated for C22H26N2O2: 350; found 351 [M+H]−, tR=2.34 min (Method 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278910B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-45a0cb3f93ca431b95cbaba6fd2ed787 |
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| Source note | uspto-grants-2016_03 |
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