HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628341Generated: October 31, 2026
Ethyl bromoacetate → HCID 67496386, compound
https://huagongshe.com/reaction/1628341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67497334 | HCID 67497334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67496386 | HCID 67496386 | 49% |
Reaction Steps
103.1.B (905 mg, 2.65 mmole), 5 ml of DMF and 0.69 ml of DIEA. The reaction mixture was cooled to 0° C., and then ethyl bromoacetate (0.49 g, 2.92 mmole) was added to the mixture. The reaction was stirred at room temperature overnight. After then, the solution was poured into saturated ammonium chloride, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. After concentration in vacuo, the residue was chromatographed on silica gel to give 103.1.C (552 mg, 49% yield) as orange syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785468B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ef2d8949056740e0a47fde76d6e005a8 |
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| Source note | uspto-grants-2014_07 |
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