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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325713Generated: October 26, 2026

Carbon Disulfide → [3-[3-(1-Piperidinylmethyl)phenoxy]propyl]isothiocyanate

https://huagongshe.com/reaction/325713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
Reactant3-(1-Piperidinylmethyl)phenoxy propanamineHCID 21297576—
CatalystMercuric ChlorideHCID 24085—
SolventAcetoneHCID 180—
Product[3-[3-(1-Piperidinylmethyl)phenoxy]propyl]isothiocyanateHCID 13391620—

Reaction Conditions

Temperature-14 °C

Reaction Steps

A solution of carbon disulphide (3.3 ml) in acetone (8 ml) was added dropwise to a solution of 3-[3-(1-piperidinylmethyl)phenoxy propanamine (12.4 g) in acetone (30 ml) over a 15 minute period, between -5° and -10° C. The solution was cooled to -14° C. and mercury (II) chloride (13.6 g) in acetone (30 ml) was added, during 45 minutes. Triethylamine (16 ml) was added at 0° C. during 15 minutes, and the mixture was heated at reflux for 45 minutes. The resulting suspension was purified by filtration and the filtrate evaporated in vacuo. The residue was purified by column chromatography using methanol as eluant to give the title compound (6 g) as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04442110
Source datasetuspto-grants-1984_04
ORD IDord-7e9628edab16419cb23c7252de072493
Source noteuspto-grants-1984_04