HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356331Generated: October 29, 2026
Ethyl bromoacetate → HCID 22396804, compound
https://huagongshe.com/reaction/1356331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22396908 | HCID 22396908 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22396804 | HCID 22396804 | 97.1% |
Reaction Steps
Sodium hydride (60% dispersion in mineral oil, 0.85 g, 21 mmol) was added to a solution of tert-butyl 7,10-dichloro-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate (5.0 g, 14 mmol) in DMF (75 mL). After 25 min, ethyl bromoacetate(3.1 mL, 28 mmol) was added. The reaction was quenched with saturated aqueous NH4Cl after 3 h and extracted with EtOAc (3×100 mL). The combined organic extracts were washed with brine, dried over Na2SO4, decanted, and concentrated. The crude product was purified by column chromatography with heptane/EtOAc (3:1) to give 6.0 g (96%) of a white foam: mp 118.5-119.5° C.; IR (diffuse reflectance) 2976, 1747, 1674, 1477, 1457, 1420, 1405, 1370, 1366, 1344, 1254, 1200, 1165, 1111, 930 cm−1; MS (EI) m/z 440 (M+), 386, 384, 339, 310, 305, 300, 298, 224, 57, 56; Anal. Calcd for C21H26Cl2N2O4: C, 57.15; H, 5.94; N, 6.35; found: C, 57.27; H, 6.01; N, 6.22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586421B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-9b315cadb29541eebb80c02cb64ab5f2 |
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| Source note | uspto-grants-2003_07 |
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