HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448194Generated: October 30, 2026
Benzyl bromoacetate → HCID 68769595, compound
https://huagongshe.com/reaction/448194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 68738533 | HCID 68738533 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | HCID 68769595 | HCID 68769595 | — |
Reaction Steps
To a stirred solution of 3-Acetylphenyl 2,6-dimethylbenzoate (Step B, 2.90 g, 10.8 mmol) in dry THF (50 ml) and DMPU (17 ml) was added a solution of lithium bis(trimethylsilyl) amide (1.0M, 11.89 ml) at −65° C. under argon. After 10 minutes of stirring at −65° C., benzyl bromoacetate (3.72 g, 16.24 mmol) was added rapidly. The reaction mixture was stirred for an additional 10 minutes and then warmed to room temperature for 4 hours. The crude mixture was taken in ethyl acetate and washed with water and brine. The aqueous layer was extracted one more time with ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (hex: ethyl acetate, 4:1) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481595B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-03224fd78dd9415c83c019b6039707eb |
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| Source note | uspto-grants-2013_07 |
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