HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628784Generated: October 29, 2026
Chloroacetyl chloride → 5-Chloromethyl-3-naphthalen-2-yl-[1,2,4]oxadiazole
https://huagongshe.com/reaction/628784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178513226 | HCID 178513226 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 5-Chloromethyl-3-naphthalen-2-yl-[1,2,4]oxadiazole | HCID 54847516 | 21.4% |
Reaction Steps
A solution of N-Hydroxy-naphthalene-2-carboxamidine (364 mg, 1.95 mmol) in dichloroethane (6 mL) and DIEA (683 μL, 3.91 mmol) was treated with a solution of chloroacetyl chloride (157 μL, 2.350 mmol) in dichloroethane (2 mL) which was added dropwise to the reaction vessel at room temperature. After the addition, the reaction mixture was heated at 50° C. for 4 hours. The reaction mixture was then concentrated to dryness and redissolved in dichloromethane. The organic layer was washed with saturated aqueous NaHCO3 and brine, respectively. The organic layer was dried over anhydrous Na2SO4, concentrated onto silica gel and purified by flash chromatography (0-50% ethyl acetate/hexanes gradient) to afford the required intermediate, 5-chloromethyl-3-naphthalen-2-yl-[1,2,4]oxadiazole (102 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315449B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-2eaf408525ce45c39b0103b37169fa96 |
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| Source note | uspto-grants-2016_04 |
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