HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521645Generated: October 26, 2026
Tributylstannane → 5-chloro-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/reaction/1521645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 3-Chloro-2-iodoaniline | HCID 21328946 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-chloro-3,4-dihydroquinolin-2(1H)-one | HCID 19027736 | — |
Reaction Steps
To a stirred solution of 3-chloro-2-iodoaniline (143-3; 1.1 g, 0.0043 mol), AIBN (0.282 g, 0.0017 mol), tributyl tinhydride (1.8 g, 0.0064 mol) in dimethyl sulphoxide (10 mL) was added ethylacrylate (1.7 g, 0.173 mol) portion wise at 0° C. Reaction mixture was allowed to stir at 120° C. for 12 h. The reaction mixture was diluted with ice cold water (150 mL) and extracted with ethyl acetate (4×100 mL). The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under vacuum to obtain the title compound. 1H NMR (400 MHz, CDCl3) δ 7.159-7.119 (t, J=7.6 Hz, 1H), 7.021-7.002 (d, J=7.6 Hz, 1H), 6.819-6.800 (d, J=7.6 Hz, 1H), 2.941-2.651 (t, J=8 Hz, 4H). MS (M+1): 181.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073929B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-2f15a7fe4ec9439ea998c3a5649177e8 |
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| Source note | uspto-grants-2015_07 |
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