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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251622Generated: November 1, 2026

Dimethyl Sulfoxide → Benzothiazole

https://huagongshe.com/reaction/2251622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant2-AminothiophenolHCID 8713—
Reactant7-Bromo-9,9-diethylfluorene-2-carboxaldehydeHCID 15476349—
SolventWaterHCID 962—
ProductBenzothiazoleHCID 722280.3%

Reaction Conditions

Temperature195 °C

Reaction Steps

A mixture of 9,9-diethyl-7-bromo-fluorene-2-carboxaldehyde (49.35 g., 0.15 mol.), 2-aminothiophenol (20 ml. 0.187 mol., 1.25 eq.), and DMSO (110 nl) was heated in an oil bath to a bath temperature of 195° C., held there for 45 minutes, and then poured into water. The separated solids were collected, reslurried in 1:4 acetic acid-water (1000 ml.) filtered, and washed with water and dilute sodium bicarbonate solution. These solids, 80.05 g., were then reslurried in hot ethanol, (600 ml), cooled and filtered to get the product benzothiazole, 45.69 g., m.p. 133.6-135° C. An additional 6.6 g., m.p. 134.6-135.5° C., was obtained by chromatography of the ethanol filtrate. Total recovery was 52.29 g. (80.3% yield). Mass Spec: m/z 433, 435, (M+). Anal. Calcd for C24H20BrNS: C, 66.37; H, 4.64; Br, 18.40; N, 3.23; S 7.37%. Found: C, 66.46; H, 4.52; Br, 18.54; N, 3.14; S, 7.19%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319151B1
Source datasetuspto-grants-2008_01
ORD IDord-b871d7960960449d875843d763702afd
Source noteuspto-grants-2008_01