HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764874Generated: October 26, 2026
Thionyl Chloride → 2-(2-Chloroethyl)isoindolin-1-one
https://huagongshe.com/reaction/1764874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(2-hydroxyethyl)-3H-isoindol-1-one | HCID 220105 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Chloroethyl)isoindolin-1-one | HCID 2783514 | 92% |
Reaction Steps
To a solution of 2-(2-hydroxyethyl)isoindolinone (1.0 g, 5.64 mmol) in toluene (3.5 mL) was added thionyl chloride (1.34 g, 11.3 mmol). The reaction mixture was stirred at 20° C. for 3 h then 4 h at 60° C. The reaction mixture was concentrated in vacuo to remove excess thionyl chloride and toluene. 2-(2-Chloroethyl)isoindolinone (1.01 g, 92%) was obtained by flash chromatography on a silica gel column by elution with EtOAc/Hexanes a white solid. 1H NMR (CDCl3, 300 MHz) δ3.81 (t, 2H, J=5.5 Hz), 3.97 (t, 2H, J=5.9 Hz), 4.59 (s, 2H), 7.44-7.58 (m, 3H), 7.86 (d, 1H, J=6.9 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039679E1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-933a6a5ec3aa4fac87abdffadc97335d |
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| Source note | uspto-grants-2007_06 |
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