HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456299Generated: November 1, 2026
Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde
https://huagongshe.com/reaction/1456299
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dihydrobenzofuran | HCID 10329 | — |
| Reactant | Bis(1,3-dichloroisopropyl ether) | HCID 93323 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dihydrobenzofuran-5-carboxaldehyde | HCID 735901 | — |
Reaction Steps
A solution of 9.4 ml (83.4 mmole) 2,3-dihydrobenzofuran in 250 ml methylene dichloride was cooled under nitrogen to 0° to -5° C. and 18 ml (167 mmole)titanium tetrachloride was added dropwise at 0° C. The resulting brown mixture was stirred 10 minutes and 8.3 ml (91.6 mmole) 1,1-dichloromethyl methylether was then added dropwise at 0° C. During this addition the reaction mixture became dark red. The mixture was allowed to warm to room temperature, stirred for two hours and poured slowly into a 2 liter beaker containing 700 ml saturated aqueous sodium bicarbonate solution. The resulting mixture was filtered through diatomaceous earth and the solids washed with methylene dichloride. The separated organic layer was dried (Na2SO4) and the solvent evaporated to afford a residual oil, log (81%) of which appeared homogeneous on silica gel TLC, eluting with an ethyl acetate/hexane/5% acetic acid 1:5:5 by volume. Mass spectrum (m/e): 148 (M+), 147, 119.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05843970 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-29e89336c8b14926a68807c194322af3 |
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| Source note | uspto-grants-1998_12 |
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