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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581868Generated: November 1, 2026

Dithiooxamide → 2,5-Bis(7-bromo-9,9-didecylfluoren-2-yl)-1,3-thiazolo(5,4-d)1,3-thiazole

https://huagongshe.com/reaction/1581868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDithiooxamideHCID 2777982—
ReactantHCID 22723474HCID 22723474—
SolventDimethyl SulfoxideHCID 679—
Product2,5-Bis(7-bromo-9,9-didecylfluoren-2-yl)-1,3-thiazolo(5,4-d)1,3-thiazoleHCID 8596666615.1%

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 7-bromo-9,9-didecylfluorene-2carbaldehyde (example 2; 6.6 g, 12 mmol), dithiooxamide (rubeanic acid, 0.6 g, 5 mmol) and DMSO (4 mL) was heated in an oil-bath to a bath temperature of 190° C., held 1 hour and poured onto water. The mixture was extracted into toluene (200 mL). The toluene extract was washed with water, dried and concentrated. The resulting residue was chromatographed over alumina to get a mixture of product containing the aldehyde product. The mixture was rechromatographed over silica gel, and elution with toluene gave 0.9 g (15% yield) of the product which was recrystallized from a mixture of heptane and hexanes to get pure product 0.6 g, (10% yield), m.p. 150.8-152.7° C. Mass Spec.(m/z): 1186, 1188, 1190 (M+). Anal. Calcd. for C70H96Br2N2S2: C, 70.68%; H, 8.14%; N, 2.36%; S, 5.39%; Br, 13.44%. Found: C, 70.69%; H, 8.22%; N, 2.07%; S, 5.31%; Br, 13.67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730793B1
Source datasetuspto-grants-2004_05
ORD IDord-b15f85af20af4d5b97c42fd0b5a6dcc1
Source noteuspto-grants-2004_05