HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376996Generated: October 25, 2026
Water → 5-Acetoxy-4,6-di-tert-butyl-2-formylbenzofuran
https://huagongshe.com/reaction/1376996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-Acetoxy-4,6-di-tert-butylbenzofuran | HCID 11822332 | — |
| Product | 5-Acetoxy-4,6-di-tert-butyl-2-formylbenzofuran | HCID 22918669 | 86% |
Reaction Steps
Phosphorus oxychloride (1.1 g) was added dropwise to N,N-dimethylformamide (0.4 g) under cooling with ice and, subsequently, a solution of 5-acetoxy-4,6-di-tert-butylbenzofuran (1.0 g) in N,N-dimethylformamide (2 ml) was added dropwise. The mixture was stirred first at room temperature for 20 min, then under heating at 80° C. for 75 min. After cooling, the reaction mixture was poured into water and subjected to extraction ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butyl-2-formylbenzofuran [0.95 g (yield, 86%)] as a colorless, fine-grained crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663373 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-1f8dc7ff76d0497f910a3ff59586e23e |
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| Source note | uspto-grants-1997_09 |
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