HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474399Generated: October 30, 2026
Diisobutylaluminum hydride → 6-bromo-5-methoxy-3,4-dihydro-1H-isochromene-1-carbaldehyde
https://huagongshe.com/reaction/1474399
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 6-bromo-N-methyl-N,5-bis(methyloxy)-3,4-dihydro-1H-isochromene-1-carboxamide | HCID 86647322 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-bromo-5-methoxy-3,4-dihydro-1H-isochromene-1-carbaldehyde | HCID 77231247 | — |
Reaction Steps
To a solution of 6-bromo-N-methyl-N,5-bis(methyloxy)-3,4-dihydro-1H-isochromene-1-carboxamide (300 mg, 0.9 mmol) in 20 mL of anhydrous THF was cooled to −30° C. and then DIBAL-H (1.3 mL, 1.3 mmol, 1M) was added. The mixture was stirred at −30° C. for 2 hours. The reaction was quenched with water and extracted with DCM. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The crude 6-bromo-5-(methyloxy)-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 | US09018211B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-b450afb7d6e149eeabee3f7502b7e991 |
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| Source note | uspto-grants-2015_04 |
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