HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322526Generated: October 30, 2026
Ethyl bromoacetate → HCID 54537755, compound
https://huagongshe.com/reaction/322526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 54130332 | HCID 54130332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54537755 | HCID 54537755 | — |
Reaction Steps
To a solution of 13-7 (1.83 g, 8.4 mmol) in THF (22 mL) at −78° C. was added sodium bis(trimethylsilyl)amide (9.4 mL, 9.4 mmol; 1M/THF) dropwise. After an additional 20 min, ethyl bromoacetate (1.13 mL, 10.3 mmol) was added dropwise. After an additional 20 minutes, the mixture was allowed to warm to 0° C., and 20 mL sat. aqueous NH4Cl was added. The layers were separated, the aqueous layer washed with EtOAc, and the combined organic extracts were dried over K2CO3. Following evaporative removal of the solvent, the residue was chromatographed (silica gel, 40% ethyl acetate/hexanes) to give 13-8 as a colorless 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-779a806be33f4024841d916c465fe753 |
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| Source note | uspto-grants-2001_04 |
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