HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414866Generated: November 1, 2026
Sodium hydride → 1-(4,5-Dihydro-2-thiazolyl)-1,3-dihydro-3-(2-thienylmethylene)-2H-indol-2-one
https://huagongshe.com/reaction/1414866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloroethyl Isothiocyanate | HCID 138661 | — |
| Reactant | 3-[(Thien-2-yl)methylene]-2-indolinone | HCID 308717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4,5-Dihydro-2-thiazolyl)-1,3-dihydro-3-(2-thienylmethylene)-2H-indol-2-one | HCID 53680413 | — |
Reaction Steps
To a stirred suspension of NaH (0.51 gm; 21.1 mmole) in dry tetrahydrofuran (100 ml) is added dropwise a solution of 3-(2-thienylmethylene)-indolin-2-one prepared as described above (4.0 gm; 17.6 mmole) in dry tetrahydrofuran (100 ml). The resultant solution is stirred at room temperature for another hour, after which, it is cooled to 0° C in an ice bath, and a solution of chloroethylisothiocyanate (2.2 gm; 17.6 mmole) in dry tetrahydrofuran (50 ml) is added. The mixture is then heated at reflux temperature for 3.5 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04002749 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-6c537529e821401cb493e0ebe8fccf11 |
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| Source note | uspto-grants-1977_01 |
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