HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690916Generated: October 25, 2026
Dimethylformamide → 4-(Butoxymethyl)benzaldehyde
https://huagongshe.com/reaction/1690916
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-4-(butoxymethyl)benzene | HCID 11402253 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Butoxymethyl)benzaldehyde | HCID 59255339 | 81.3% |
Reaction Steps
To a solution of 1-bromo-4-butoxymethyl-benzene (11.5 g, 47.3 mmol) described in Manufacturing Example 4-1-1 in tetrahydrofuran (200 mL) was added n-butyl lithium (32.5 mL, 1.6 M hexane solution, 52.0 mmol) at −78° C. This mixture was stirred for 55 minutes at −78° C., and N,N-dimethylformamide (4.4 mL, 56.8 mmol) was added thereto at −78° C. This mixture was warmed to room temperature, and stirred for 20 minutes. The reaction solution was partitioned into water and ethyl acetate at 0° C. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1) to obtain the title compound (7.39 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153662B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-6cd975db1296411eb86b6abb212f81cc |
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| Source note | uspto-grants-2012_04 |
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