HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402784Generated: October 26, 2026
Water → 4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene-6-carbaldehyde
https://huagongshe.com/reaction/402784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 6-bromo-4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene | HCID 45255972 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene-6-carbaldehyde | HCID 77230776 | — |
Reaction Steps
6-Bromo-4,4-dimethyl-8-(propan-2-yl)-3,4-dihydro-2H-chromene (154 mg, 0.54 mmol) in tetrahydrofuran (5.44 mL) was cooled to −78° C. and n-BuLi (261 μL, 0.65 mmol) was added dropwise via a syringe. The reaction mixture was stirred at −78° C. for 30 minutes, and then DMF (168 μL, 2.17 mmol) was added dropwise. The resulting mixture was allowed to warm to room temperature, and stirred for 30 minutes before water was added. It was then extracted with EtOAc (2×) and the combined organic layers were dried over Na2SO4, filtered, and concentrated under vacuum. The crude residue was purified by silica gel chromatography eluting with 0-10% EtOAc/Hexanes to obtain the desired product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742110B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-1d3fe5d735954dee874792b29cde22b3 |
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| Source note | uspto-grants-2014_06 |
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