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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836743Generated: October 30, 2026

Phenyl Isothiocyanate → N-(3-(Dimethylamino)propyl)-N'-phenylthiourea

https://huagongshe.com/reaction/1836743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl IsothiocyanateHCID 7673—
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
SolventIsopropanolHCID 3776—
Solventtert-Butyl methyl etherHCID 15413—
ProductN-(3-(Dimethylamino)propyl)-N'-phenylthioureaHCID 198245970.1%

Reaction Steps

Phenyl isothiocyanate (5.283 g, 39.1 mmole) in 30 mL t-butyl methyl ether was added to a solution of 3-(dimethylamino)propylamine (3.993 g, 39.1 mmole) in 10 mL isopropanol. After stirring 2 hr at room temp., the solid which separated was filtered out and washed with t-butyl methyl ether to afford 6.51 g of 1-[3-(dimethylamino)propyl]-3-phenylthiourea (mp 112-114° C.), part of which (2.374 g, 10 mmole) was dissolved in ethanol (20 mL) containing conc. HCl (1.67 mL, 20 mmole) and added to 2-methylnaphthoquinone dissolved in warm ethanol (35 mL). After 4 days in a stoppered flask at room temp., the mixture was concentrated, and dissolved in ethyl acetate. The solid which separated after 16 hr was filtered out, but became sticky on the filter and was discarded. The filtrate was stored another 12 days at room temp. The powder which separated was filtered out to give 600 mg of pinkish-buff powder. Of this, 325 mg was recrystallized from 10 mL methanol+60 mL ethyl acetate containing a few drops of water to give 260 mg of the title compound, mp 238-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777557B2
Source datasetuspto-grants-2004_08
ORD IDord-da8dcba9b8194a44ac4326c387700005
Source noteuspto-grants-2004_08