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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044478Generated: October 31, 2026

Ethyl chloroformate → HCID 57471166, compound

https://huagongshe.com/reaction/1044478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 57467188HCID 57467188—
SolventPyridineHCID 1049—
ProductHCID 57471166HCID 57471166—

Reaction Steps

To 1-(3,4-dichlorobenzyl)-7-methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochloride (1.95 g, 5.80 mmol) in pyridine 10 ml) the ethylchloroformate (1.00 g, 9.28 mmol) was added slowly under nitrogen. The mixture was stirred over night at RT. The solvent was reduced under vacuo and extracted with CH2Cl2 after addition of HCl (1N). The organic layer was washed with HCl (1N), NaHCO3 solution, and NaCl solution, then dried on MgSO4 and the solvent was removed. The product was obtained as an orange oil that precipitates after a few hours (2.10 g, 5.14 mmol, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563617B2
Source datasetuspto-grants-2013_10
ORD IDord-d030d44b4d904fcfac76d117a657a7c8
Source noteuspto-grants-2013_10