HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217321Generated: October 29, 2026
Bromotrichloromethane → HCID 67234103, compound
https://huagongshe.com/reaction/2217321
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromotrichloromethane | HCID 6383 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 43405688 | HCID 43405688 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67234103 | HCID 67234103 | — |
Reaction Steps
DAST (diethylaminosulfur trifluoride) was added to a cold (−78° C.) solution of 3-hydroxy-2-[2-(4-methoxy -phenyl)-acetylamino]-propanoic acid methyl ester (400 mg, 1.5 mmol) in dichloromethane (8 mL). After stirring for 1 h at −78° C., CCl3Br (149 μL, 1.5 mmol) and DBU (226 μL, 1.5 mmol) were added and the reaction was allowed to warm to 25° C. and stirred at this temperature for 12h. The reaction was poured into saturated aqueous NaHCO3 and the biphasic mixture was extracted with DCM. The combined organic extracts were dried with MgSO4 and purified by column chromatography (hexanes: ethyl acetate from 25 to 100%). 2-(4-Methoxy-benzyl)-oxazole-4-carboxylic acid methyl ester was isolated as a white solid (80 mg, 21%). ESI-MS m/z calc. 247.5, found 248.2 (M+1)+. Retention time of 2.64 minutes. 1H NMR (400 MHz, CDCl3) δ3.80 (s, 3H), 3.92 (s, 3H), 4.12 (s, 2H), 6.87 (d, J=8.0 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407976B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-f2b898158ef642cc97189f5982bd392e |
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| Source note | uspto-grants-2008_08 |
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