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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593369Generated: October 30, 2026

Hydrochloric Acid → (R)-5-(5-amino-2-fluoro-phenyl)-5-methyl-morpholine-3-thione hydrochloride

https://huagongshe.com/reaction/593369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(R)-5-[5-(Benzhydrylidene-amino)-2-fluoro-phenyl]-5-methyl-morpholine-3-thioneHCID 86651220—
Solvent1,4-DioxaneHCID 31275—
Product(R)-5-(5-amino-2-fluoro-phenyl)-5-methyl-morpholine-3-thione hydrochlorideHCID 8666799387%

Reaction Steps

A solution of (R)-5-[5-(benzhydrylidene-amino)-2-fluoro-phenyl]-5-methyl-morpholin-3-thione (0.795 g, 1.97 mmol) in dioxane (10 ml) was treated dropwise at room temperature with hydrochloric acid (1M). The yellow reaction mixture was stirred at room temperature overnight. For the workup, the solution was evaporated at reduced pressureand. The yellow oil was dissolved in ether (15 ml), and the solution was extracted with hydrochloric acid (1M, 15 ml). The aqueous layer was extracted with ether (15 ml), then the combined organic layers were extracted with hydrochloric acid (1M, 5 ml). The combined aqueous layers were evaporated at reduced pressure and yielded the (R)-5-(5-amino-2-fluoro-phenyl)-5-methyl-morpholine-3-thione hydrochloride as a yellow solid (0.47 g, 87%) which was pure enough to be engaged in the next step without further purification; (calculated) C11H13FN2OS [240.30]; (found) [M+H]+=241.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242943B2
Source datasetuspto-grants-2016_01
ORD IDord-1c9e7c26bbf04ce4aac68bb82fdc6956
Source noteuspto-grants-2016_01