HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889714Generated: October 30, 2026
Diisobutylaluminum hydride → HCID 39232332, compound
https://huagongshe.com/reaction/1889714
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 58531623 | HCID 58531623 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 39232332 | HCID 39232332 | 87.1% |
Reaction Steps
4′,6-Dichloro-N-methoxy-N-methylbiphenyl-3-carboxamide (1.0 g, 3.2 mmol, 1.0 eq) was dissolved in dry THF and stirred for 10 minutes. The solution was cooled to −78° C. and DIBAL-H (1 M solution, 1.83 g, 12.9 mmol, 4 eq, 13 mL) was slowly added over 15-30 minutes. The reaction mixture was stirred for 1 h at −78° C., quenched with saturated NH4Cl solution at −78° C. and stirred for 30 minutes at ambient temperature. Water and ethyl acetate were added into the reaction mixture. The aqueous layer was separated and extracted twice with ethyl acetate. The organic layer was dried with anhydrous Na2SO4 and concentrated under vacuum to give the desired product (0.7 g, 87%). 1H NMR (400 MHz, CDCl3) δ 7.06-7.09 (d, 2H), 7.24-7.27 (d, 2H), 7.40 (s, 1H), 7.55-7.58 (d, 1H), 7.90-7.95 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501992B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-2f5ba791826e4ac0b37ff84529f555f9 |
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| Source note | uspto-grants-2013_08 |
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