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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625872Generated: October 30, 2026

Iodine → HCID 90456722, compound

https://huagongshe.com/reaction/625872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactantmethyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoateHCID 10903591—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant5-Bromo-1,3-dichloro-2-fluorobenzeneHCID 22926230—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 90456722HCID 90456722—
ProductHCID 90456910HCID 90456910—

Reaction Steps

To an oven dried 8 mL vial with teflon cap purged with N2 was added Zinc dust (298 mg, 4.56 mmol), DMF (1.5 mL), and iodine (57.8 mg, 0.228 mmol). To this mixture was added (R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate (500 mg, 1.519 mmol), immediately followed by iodine (57.8 mg, 0.228 mmol). Pd2(dba)3 (69.6 mg, 0.076 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (62.4 mg, 0.152 mmol), 5-bromo-1,3-dichloro-2-fluorobenzene (556 mg, 2.279 mmol) and the reaction mixture was allowed to stir at rt for 16 h. The crude mixture was diluted in 30 mL of EtOAc and DMF was removed using four aqueous washes. The organic phase was dried over anhydrous sodium sulfate. The solution was filtered and concentrated and the crude product was purified by silica gel chromatography using 100% hexanes to 30% EtOAc/Hexanes. The desired product was obtained as a pale yellow oil, (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(3,5-dichloro-4-fluorophenyl)propanoate, 0.102 g which was taken into next step directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308236B2
Source datasetuspto-grants-2016_04
ORD IDord-564cd7e2d0624118a904646381e4cfdd
Source noteuspto-grants-2016_04