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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-Butyl ((tert-butoxycarbonyl)amino)acetateHCID 4097102—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoateHCID 57611911—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168658B2
Source datasetuspto-grants-2012_05
ORD IDord-fd8c5cc610c84a5b9d787fb783e8e6d1
Source noteuspto-grants-2012_05