HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173265Generated: October 30, 2026
Diisobutylaluminum hydride → 5-bromo-3,4-dihydro-1H-isochromene-1-carbaldehyde
https://huagongshe.com/reaction/2173265
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 5-bromo-N-methyl-N-(methyloxy)-3,4-dihydro-1H-isochromene-1-carboxamide | HCID 86647310 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-bromo-3,4-dihydro-1H-isochromene-1-carbaldehyde | HCID 77231248 | — |
Reaction Steps
A solution of 5-bromo-N-methyl-N-(methyloxy)-3,4-dihydro-1H-isochromene-1-carboxamide (3.0 g, 10 mmol) in 60 mL of anhydrous THF was cooled to −30° C. and then DIBAL-H (20 mmol) was added. The mixture was stirred at −30° C. for 1 hours. The reaction was quenched with water, extracted with DCM. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The crude 5-bromo-3,4-dihydro-1H-isochromene-1-carbaldehyde was used for next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056859B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d9f4cfa9e4474008a9540fd49d0de689 |
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| Source note | uspto-grants-2015_06 |
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