Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871162Generated: November 4, 2026

Dimethyl Sulfoxide → Benzothiazole

https://huagongshe.com/reaction/1871162

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-amino thiophenol (20 ml. 0.187 mol., 1,25 eq.), and DMSO (110 ml) 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 52.29 g. (80.3% yield). Mass Spec: m/z 433, 435, (M+). Analysis calculated 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 numberUS06100405
Source datasetuspto-grants-2000_08
ORD IDord-6f7045a8391349eda2ff9383fef76673
Source noteuspto-grants-2000_08