HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362272Generated: October 25, 2026
Lithium diisobutylaluminum hydride → HCID 59277551, compound
https://huagongshe.com/reaction/1362272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium diisobutylaluminum hydride | HCID 22042274 | — |
| Reactant | HCID 59277598 | HCID 59277598 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59277551 | HCID 59277551 | 56% |
Reaction Steps
Diisobutylaluminum lithium hydride (30.7 mL of a 1.0 M in hexanes, 30.7 mmol) was added dropwise to an ice-cold solution of 3-chloro-2-propoxybenzoic acid propyl ester (2.63 g, 10.2 mmol) in THF (20 mL). After the addition was complete, the ice bath was removed and the mixture stirred at ambient temperature for 18 h. The reaction was cooled to 0° C. and HCl (1N, 100 mL) was added until all the resulting solids returned to solution. The solution was extracted with Et2O (3×100 mL). The combined organics were washed with brine (2×100 mL), dried (Na2SO4) filtered and concentrated to yield the title compound (1.12 g, 56%) as a light yellow oil: 1H NMR (500 MHz, DMSO-d6) δ 7.40-7.33 (m, 2H), 7.13 (t, J=7.7 Hz, 1H), 5.22 (t, J=5.6 Hz, 1H), 5.56 (d, J=5.6 Hz, 2H), 3.84 (t, J=6.4 Hz, 2H), 1.76-1.71 (m, 2H), 1.01 (t, J=7.3 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879872B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-4e93f43cdfbb43f481a1c6dd5cf734e3 |
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| Source note | uspto-grants-2011_02 |
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