HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751344Generated: October 30, 2026
Dimethylformamide → HCID 86035948, compound
https://huagongshe.com/reaction/751344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1-(Thiophen-3-yl)-1,3-dihydro-2H-indol-2-one | HCID 14819378 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86035948 | HCID 86035948 | 57% |
Reaction Steps
Phosphorous oxychloride (1.9 mL, 20.9 mmol) is added slowly to a stirred solution of dimethylformamide (2 mL) and dichloromethane (2 mL) cooled to 0-5° C. After 5 min a solution of the above 1-(thien-3-yl)-1H-indol-2-one (1.0 g, 2.65 mmol), pyridine (1 mL) and dichloromethane (4 mL) is added and the reaction is stirred at room temperature for 48 hr. The reaction mixture is poured into ice/water and extracted with ethyl acetate. Some solids are removed by filtration and the organic layer is separated, dried, filtered and concentrated. The residue is purified by chromatography eluting with pentane-10% ethyl acetate. Product containing fraction are combined and concentrated to afford 2-chloro-1-(thien-3-yl)-1H-indole-3-carboxaldehyde (694 mg, 57%) as a light orange solid. MS 262 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405300B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-7d96ce2a87f44694af38317b0cdf6d5e |
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| Source note | uspto-grants-2008_07 |
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