HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602636Generated: November 2, 2026
Ethyl bromoacetate → HCID 53687702, compound
https://huagongshe.com/reaction/1602636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 18394796 | HCID 18394796 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53687702 | HCID 53687702 | — |
Reaction Steps
To a stirred solution of 11-7 (355 mg, 1.67 mmol) and THF (10 mL) at -78° C. was added NaN(TMS)2 (1.83 mL, 1.83 mmol, 1.0M in THF). After 20 min, ethyl bromoacetate (0.203 mL, 1.84 mmol) was added and the reaction was warmed to 0° C. After 30 minutes, the reaction mixture was diluted with EtOAc and then washed with H2O, brine, dried (MgSO4), and concentrated to give 11-8 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05981546 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-165adbd6e64945fea0befb1a1a961eca |
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| Source note | uspto-grants-1999_11 |
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