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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356202Generated: November 1, 2026

Benzyl Bromide → HCID 11488850, compound

https://huagongshe.com/reaction/1356202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(tert-Butoxycarbonyl)-3-iodo-L-tyrosineHCID 15545208—
ReactantEthyl acetate hexaneHCID 21226206—
SolventEthyl AcetateHCID 8857—
ProductHCID 11488850HCID 11488850—

Reaction Conditions

Temperature90 °C

Reaction Steps

(2S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-3-iodo-phenyl)-propionic acid (490 mg. 1.2 mmol) of Step A is stirred in EtOAc (3.6 mL) with DIEA (418 μL, 2.4 mmol) at RT under N2. Benzyl bromide (171 μL, 1.44 mmol) is then added and the reaction mixture is then heated to 90° C. overnight. TLC in 3/1 hexane/EtOAc shows complete consumption of starting material (ninhydrin positive) and the appearance of two higher rf spots. The reaction is cooled to RT, diluted with EtOAc and washed with 1N HCl (2×30 mL) and with saturated NaHCO3 (2×30 mL). The organics are dried (MgSO4), filtered and concentrated to provide a mixture of mono- and dibenzylated products. Flash chromatography (3:1 hexane/EtOAc) affords the title compound, (2S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-3-iodo-phenyl)-propionic acid benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586467B2
Source datasetuspto-grants-2003_07
ORD IDord-a30a2d0ebd524706808224d26c80fdfd
Source noteuspto-grants-2003_07