HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211517Generated: October 31, 2026
Water → 2(3H)-Benzoxazolone, 3-(3-chloropropyl)-
https://huagongshe.com/reaction/2211517
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2(3H)-Benzoxazolone | HCID 6043 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2(3H)-Benzoxazolone, 3-(3-chloropropyl)- | HCID 10036072 | — |
Reaction Steps
To a stirred suspension of sodium hydride (7.8 g, 0.16 mol, ether-washed) in dimethylformamide (75 ml) was added dropwise under nitrogen, 2-benzoxazolinone (20.0 g, 0.15 mol) dissolved in dimethylformamide (150 ml). After complete addition the reaction was stirred at ambient temperature for 30 min. and then it was cooled to −5° C. with an ice-acetone bath. A solution of 3-chloro-1-bromopropane (46.6 g, 0.30 mol) in dimethylformamide (50 ml) was added dropwise (temperature never exceeded 0° C.). The reaction was allowed to reach ambient temperature and was stirred for 16 hours. The reaction was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate was washed with water, dried (MgSO4), and the extract concentrated from toluene-hexane to afford N-(3-chloropropyl)-2-benzoxazolinone as large needles, 15.6 g, m.p.=264°-266° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039265E1 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-795037d93e7641ef88a9facb48490fc8 |
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| Source note | uspto-grants-2006_09 |
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