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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408611Generated: October 26, 2026

Benzyl Bromide → HCID 70564348, compound

https://huagongshe.com/reaction/408611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantAzetidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 14821735—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 70564348HCID 70564348—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of azetidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (1 eq.) in dry THF under Argon at −78° C. was added a solution of LiHMDS 1M in hexane (1.3 eq.). The mixture was stirred at −78° C. for 1 h, then benzyl bromide (1.3 eq.) was added. The reaction was stirred at −78° C. for 30 min, then at 0° C. for 2 h, then at 20° C. for 1 h. The crude was diluted with EtOAc, carefully hydrolyzed with a saturated aqueous solution of NH4Cl. The organic layer was washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc: 98/2 to 80/20) to afford 2-benzyl-azetidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-920fcf7c4cf84573a964ea9bbc87fd21
Source noteuspto-grants-2014_06