HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322520Generated: October 30, 2026
Ethyl bromoacetate → HCID 53774644, compound
https://huagongshe.com/reaction/322520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 18394801 | HCID 18394801 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53774644 | HCID 53774644 | — |
Reaction Steps
To a stirred solution of 12-3 (210 mg, 0.7257 mmol) and THF (5 mL) at −78° C. was added NaN(TMS)2 (0.943 mL, 0.943 mmol, 1.0 M in THF). After 30 min, ethyl bromoacetate (0.104 mL, 0.9434 mmol) was added and the reaction was warmed to 0° C. After 1.0 hour, the reaction mixture was diluted with EtOAc and then washed with sat NaHCO3, brine, dried (MgSO4), and concentrated to give 12-4 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211184B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-07d07bb2043c4ca69857eef5c6a033b5 |
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| Source note | uspto-grants-2001_04 |
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