HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107528Generated: October 30, 2026
Dimethyl Sulfoxide → 2,3-Dihydro-1-benzofuran-4-carbaldehyde
https://huagongshe.com/reaction/1107528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2,3-Dihydro-1-benzofuran-4-yl)methanol | HCID 18787415 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dihydro-1-benzofuran-4-carbaldehyde | HCID 18787449 | — |
Reaction Steps
DMSO (8.10 mL, 114 mmol) was added at -78° C. to a stirred solution of oxalyl chloride in CH2Cl2 (40 mL of a 2M solution). A solution of (2,3-dihydrobenzofuran-4-yl)methanol (8.53 g, 56.9 mmol) in CH2Cl2 (35 mL) was added dropwise, and the solution stirred at -78° C. for 30 min. Triethyl amine (33 mL, 228 mmol) was added cautiously to quench the reaction. The resulting suspension was stirred at room temperature for 30 min and diluted with CH2Cl2 (100 mL). The organic layer was washed three times with water, and twice with brine, and then concentrated in vacuo to an oil (8.42 g, 100%) that was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06060506 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-3e8734380d154ec2be50772cf07883dd |
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| Source note | uspto-grants-2000_05 |
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