HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108614Generated: October 31, 2026
Diisobutylaluminum hydride → HCID 11131640, compound
https://huagongshe.com/reaction/2108614
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 10904699 | HCID 10904699 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11131640 | HCID 11131640 | 100% |
Reaction Steps
To a mixture of methyl 3,5-dichloro-4-(3′-iso-propyl-4′-methoxyphenoxy)-benzoate (1.40 g, 3.37 mmol) in THF (10.0 mL) at 0° C. was added a solution of DIBAL-H (8.12 mL, 8.12 mmol, 1.0 M solution in THF). The reaction mixture was stirred at room temperature for 16 h, quenched with cold 1 N HCl and diluted with ethyl acetate. The organic layer was washed with 1 N HCl and brine, dried over MgSO4, filtered and concentrated under reduced pressure to afford 4-(3′-iso-propyl-4′-methoxyphenoxy)-3,5-dichlorobenzyl alcohol as an off-white solid (0.94 g, 100%): 1H NMR (300 MHz, DMSO-d6): δ 7.54 (s, 2H), 6.81 (m, 2H), 6.40 (m, 1H), 5.51 (m, 1H), 4.54 (d, J=6.0 Hz, 2H), 3.75 (s, 3H), 3.21 (m, 1H), 1.13 (d, J=6.0 Hz, 6H); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=hexanes-acetone (17:3); Rf=0.27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514419B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-b390d54c53cd47d09ca4b3d7b35b4db9 |
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| Source note | uspto-grants-2009_04 |
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