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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579782Generated: October 26, 2026

Carbon Disulfide → 1-Acetyl-4-(isothiocyanatomethyl)piperidine

https://huagongshe.com/reaction/579782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
Reactant1-(4-(Aminomethyl)piperidin-1-yl)ethan-1-oneHCID 12687022—
SolventTetrahydrofuranHCID 8028—
Product1-Acetyl-4-(isothiocyanatomethyl)piperidineHCID 15611590100%

Reaction Steps

To a stirred and cooled (-10° C.) mixture of 41.6 parts of N,N'-methanetetraylbis[cyclohexanamine], 101 parts of carbon disulfide and 450 parts of tetrahydrofuran was added dropwise a solution of 31.2 parts of 1-acetyl-4-piperidinmethanamine in 90 parts of tetrahydrofuran. Upon completion, stirring was continued overnight at room temperature. The reaction mixture was evaporated. 2,2'-Oxybispropane was added to the residue. The precipitate was filtered off and the filtrate was evaporated, yielding 40 parts (100%) of 1-acetyl-4-(isothiocyanatomethyl)piperidine as a residue (intermediate 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749702
Source datasetuspto-grants-1988_06
ORD IDord-1337f970bdae4f528bf07a13cbb69d57
Source noteuspto-grants-1988_06