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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226203Generated: November 1, 2026

Formaldehyde → 1-(2-Dimethylaminoethylamino)-4-(hydroxymethyl)thioxanthen-9-one

https://huagongshe.com/reaction/2226203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18947267HCID 18947267—
SolventAcetic AcidHCID 176—
ProductIsopropylamineHCID 6363—
Product1-(2-Dimethylaminoethylamino)-4-(hydroxymethyl)thioxanthen-9-oneHCID 33345864%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-[[2-(dimethylamino)ethyl]amino]thioxanthen-9-one (13 g, 0.044 mol), 37% formalin (390 mL) and 5N acetic acid (6.5 mL) was heated to 100° C. for 8.5 hours, allowed to stand over the weekend and then was heated at 100° C. for several more hours. The mixture was poured into ice water, basified with 35% NaOH and extracted with chloroform. The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica eluting in succession with; 25% CHCL3/ hexane; 50% CHCl3 /hexane; 75% CHCl3 /hexane; 100% CHCl3 ; 0.5% isopropylamine/chloroform; 1% isopropylamine/chloroform; 2% isopropylamine/chloroform; then 2% isopropylamine/2% MeOH/CHCl3 to afford 9.2 g (64%) of 1-[[2-(dimethylamino)ethyl]amino]-4-(hydroxymethyl)thioxanthen-9-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346917
Source datasetuspto-grants-1994_09
ORD IDord-aa5cc61b26a542f2a341f9f17e238f0c
Source noteuspto-grants-1994_09