HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247652Generated: October 28, 2026
Carbon tetrabromide → HCID 68525948, compound
https://huagongshe.com/reaction/2247652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl azetidine-3-carboxylate hydrochloride | HCID 44828820 | — |
| Reactant | (5-{5-[4-Phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-2-thienyl)methanol | HCID 68522049 | — |
| Product | HCID 68525948 | HCID 68525948 | — |
Reaction Steps
The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 1 (1f) using (5-{5-[4-phenyl-5-(trifluoromethyl)-2-thienyl]-1,2,4-oxadiazol-3-yl}-2-thienyl)methanol (0.12 g, 0.29 mmol) that was obtained in Example 4 (4c), carbon tetrabromide (0.19 g, 0.58 mmol), triphenylphosphine (0.15 g, 0.58 mmol), ethyl 3-azetidinecarboxylate hydrochloride (62 mg, 0.38 mmol), and N,N-diisopropylethylamine (0.13 ml, 0.73 mmol). Subsequently, the crude product of the title compound thus obtained was purified by thin layer chromatography on a silica gel plate using a mixed solvent of ethyl acetate and hexane (4:5) as the developing solvent to afford the title compound (0.12 g) in a yield of 80% as a colourless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687491B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-28b92075f6e9421d80dbcd4e02eac1b8 |
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| Source note | uspto-grants-2010_03 |
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