Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864610Generated: November 2, 2026

Hydrochloric Acid → HCID 59728830, compound

https://huagongshe.com/reaction/1864610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDimethyl(methylene)ammounium iodideHCID 2724133—
ReactantHCID 86598689HCID 86598689—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59728830HCID 59728830—

Reaction Steps

To a solution of 4-1 (24.5 g, 69.9 mmol) in 250 mL dichloromethane was added the Eschenmoser's salt (16.4 g, 174.8 mmol). The mixture was refluxed over 48 hr and then cooled to room temperature. After addition of MeI (8.7 mL, 139.8 mmol) and Et3N (24.4 mL, 174.8 mmol), the mixture was stirred at room temperature for 48 hr and concentrated. The residue was dissolved in dichloromethane (150 mL). DBU (21 mL, 139.8 mmol) was added. The mixture was stirred overnight and diluted with water (150 mL) and acidified with 6N HCl until pH=4. After removal of the solvent, the residue was extracted with EtOAc (×3). The combined organic layers was washed with brine and dried (MgSO4). Concentration of the mixture afforded a yellow solid as the desired product 4-2 which was further purified by recrystalization (methanol/water). MS calculated M-H2O: 344.5. Found 345.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625919B2
Source datasetuspto-grants-2009_12
ORD IDord-5e73b91d320343ec9261ff2eff7934e5
Source noteuspto-grants-2009_12