HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493045Generated: October 28, 2026
Dimethyl Sulfoxide → 5-Acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran
https://huagongshe.com/reaction/1493045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19078595 | HCID 19078595 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran | HCID 19078578 | 43.1% |
Reaction Steps
A solution of oxalyl chloride (0.45 ml, 4.7 mmol) in dichloromethane (10 ml) was cooled to -78° C. and dimethyl sulfoxide (1 ml) was added dropwise with stirring. After stirring at the same temperature for 2 hours, a solution of 5-acetylamino-2-hydroxymethyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran (1.1 g, 4.2 mmol) in dichloromethane (5 ml) was added dropwise and the mixture was stirred for additional 30 minutes. Triethylamine (3.5 ml) was added and the mixture was stirred for 10 minutes. The reaction mixture was washed with 1N hydrochloric acid and aqueous saturated sodium bicarbonate solution. The reaction mixture was dried and then concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate) to obtain the desired compound (0.47 g, yield: 43.1%) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05376681 |
|---|
| Source dataset | uspto-grants-1994_12 |
|---|
| ORD ID | ord-55991ef8afe94082a31f82d7ec03bc2a |
|---|
| Source note | uspto-grants-1994_12 |
|---|