HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637752Generated: October 25, 2026
Sodium hydride → 3-Acetyl-2-[2-(3-dimethylaminopropoxy)phenyl]benzothiazoline
https://huagongshe.com/reaction/637752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | 3-Acetyl-2-(2-hydroxyphenyl)benzothiazoline | HCID 13335960 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Acetyl-2-[2-(3-dimethylaminopropoxy)phenyl]benzothiazoline | HCID 13335759 | 56% |
Reaction Steps
To the suspension of 0.26 g of the sodium hydride in anhydrous DMF, the solution of 1.36 g of 3-acetyl-2-(2-hydroxyphenyl)benzothiazoline in 5 ml of anhydrous DMF is added dropwise under nitrogen atmosphere at room temperature. After the addition, the reaction mixture is stirred for 20 minutes at room temperature. To the reaction mixture, the solution of 0.61 g of 3-dimethylaminopropyl chloride in 10 ml of anhydrous DMF is added. The reaction mixture is stirred for 2 hours at 80° C., and washed with n-hexane after cooling and poured into ice-water. The separated oil is extracted with ethyl acetate. The organic layer is washed with N--NaOH solution, water and saturated sodium chloride solution in the order named and dried over anhydrous magnesium sulfate. Ethy acetate is removed off in vacuo to give 1.0 g (56%) of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04558125 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-2bc37b56090748659ea5ce9af168942d |
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| Source note | uspto-grants-1985_12 |
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