HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53239Generated: October 28, 2026
Dimethylformamide → HCID 11447610, compound
https://huagongshe.com/reaction/53239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 5-Bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furan | HCID 10779312 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11447610 | HCID 11447610 | 28.1% |
Reaction Steps
t-Butyllithium (11.9 mL, 20.3 mmol, 1.7M in pentane) is added dropwise to a solution of 5-bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furan (3.60 g, 12.7 mmol) in 50 mL of anhydrous THF at -78° C.; the resulting reaction mixture is stirred at -78° C. for 15 min and N,N-dimethylformamide (1.0 mL, 13.0 mmol) is introduced. The reaction mixture is kept at -78° C. for 0.5 h, quenched with water, warmed to room temperature, and extracted with ether. The extract is washed with water, dried over anhydrous magnesium sulfate, and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (10%→20% ether-hexane) gives 0.83 g (28%) of 7-tert-butyl-2,3-dihydro-3,3-dimethyl-5-formylbenzo[b]furan as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618835 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-8382aa719f13415ba067e4a9a410d282 |
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| Source note | uspto-grants-1997_04 |
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