HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186257Generated: November 1, 2026
Water → 5-Benzyloxy-4-t-butyl-2-formylbenzofuran
https://huagongshe.com/reaction/2186257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-Benzyloxy-4-t-butylbenzofuran | HCID 23442878 | — |
| Product | 5-Benzyloxy-4-t-butyl-2-formylbenzofuran | HCID 23442879 | 36% |
Reaction Steps
Under ice-cooling, 26.2 ml of phosphorus oxychloride was added dropwise to 17 ml of N,N-dimethylformamide, followed by a solution of 40.0 g of 5-benzyloxy-4-t-butylbenzofuran in 10 ml of N,N-dimethylformamide. After stirring at room temperature for 20 minutes, the mixture was heated at 80° C. for 2 hours. After cooling, the reaction solution was poured into water and extracted with ethyl acetate. The extracted layers were washed with a saturated aqueous sodium bicarbonate solution and then water, dried over anhydrous magnesium sulfate, and then concentrated. The concentrate was purified by silica gel column chromatography (in n-hexane containing 10%ethyl acetate) to give 16.2 g of 5-benzyloxy-4-t-butyl-2-formylbenzofuran as a pale yellow solid (yield 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403639B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-b936e20376b54177b320e5dc583d162e |
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| Source note | uspto-grants-2002_06 |
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