HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919898Generated: October 26, 2026
Methyl 4-(bromomethyl)benzoate → Methyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoate
https://huagongshe.com/reaction/1919898
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | tert-Butyl ((tert-butoxycarbonyl)amino)acetate | HCID 4097102 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoate | HCID 57611911 | — |
Reaction Steps
Tert-butyl[(tert-butoxycarbonyl)amino]acetate (1.01 g, 4.37 mmol) was dissolved in THF (10 mL) and cooled to −78° C. LiHMDS (6.5 mL, 1M solution in THF) was slowly added and allowed to stir for 30 minutes. Methyl 4-(bromomethyl)benzoate (1.98 g, 8.64 mmol) in THF (6 mL) was added to the mixture and allowed to stir overnight, slowly warming to room temperature. The reaction was diluted with ethyl acetate and quenched with saturated ammonium chloride. The aqueous layer was extracted three times with ethyl acetate. The combined organic layer was dried over sodium sulfate, filtered, and concentrated. The resulting residue was purified by column chromatography. MS: cal'd 379 (MH+), exp 402 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168658B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-fd8c5cc610c84a5b9d787fb783e8e6d1 |
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| Source note | uspto-grants-2012_05 |
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