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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588900Generated: October 25, 2026

Water → HCID 117610999, compound

https://huagongshe.com/reaction/588900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantL-AlanineHCID 5950—
Reactant2-Hydroxybenzaldehyde phenylhydrazoneHCID 249842—
Reactant1-Bromo-2-chloro-5-iodo-4-methoxybenzeneHCID 90455719—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 117610999HCID 11761099964%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-bromo-2-chloro-5-iodo-4-methoxybenzene (3 g, 8.64 mmol), (S)-2-aminopropanoic acid (769 mg, 8.64 mmol), CuI (164 mg, 0.864 mmol), 2-hydroxybenzaldehyde phenylhydrazone (366 mg, 1.73 mmol), K3PO4.3H2O (4.6 g, 17.28 mmol) in DMF (10 mL) was stirred under argon at 80° C. for 16 h. The mixture was allowed to cool to RT, H2O and Et2O were added to the solution. The resulting solution was partitioned into two phases, the aqueous phase was separated, and the organic layer was extracted with 5% NaOH. The combined aqueous phase was acidified to pH 4 with 20% HCl, and then extracted with Et2O. The resulting organic layer was dried over MgSO4 and concentrated in vacuo to afford the desired product (1.7 g, 64% yield). ESI-MS m/z: 306.1[M+H]−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-2c718b8bd3224115866d11c8b2c71dd9
Source noteuspto-grants-2016_01