HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043481Generated: October 26, 2026
Dimethylformamide → 2,6-Dichloro-4-(ethylthio)benzaldehyde
https://huagongshe.com/reaction/1043481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3,5-Dichlorophenyl ethyl sulfide | HCID 59752058 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Dichloro-4-(ethylthio)benzaldehyde | HCID 86613276 | 97.5% |
Reaction Steps
A solution of 3,5-dichlorophenyl ethyl sulfide (1.0 g, 4.8 mmol) in tetrahydrofuran (4 mL) was cooled to −78° C. A solution of n-butyllithium (4.5 mL, 1.6 M in hexane) was added dropwise and the mixture was stirred at −78° C. for 45 minutes. N,N-dimethylformamide (4.47 mL, 57.7 mmol) was added and the mixture was stirred at −78° C. for 1 hour. The mixture was stirred at room temperature for 2 hours. The mixture was quenched with ice water and extracted three times with ethyl acetate. The combined extracts were dried with sodium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel to give the desired product (1.1 g, 97%). 1H NMR (CDCl3) δ 10.40 (s, 1H), 7.20 (s, 2H), 3.00 (m, 2H), 1.4 (m, 3H). LC/MS: 235 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563541B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-3b93899ba83d4b91b0ba8ae530658e34 |
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| Source note | uspto-grants-2013_10 |
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