(2-Chlorophenyl)(2,2-diethoxyethyl)sulfane → 7-Chloro-1-benzothiophene

Into a 2 L round bottomed flask is added 2-chlorobenzenethiol (50.0 g, 346 mmol), potassium carbonate (52.7 g, 381 mmol) and acetone (1 L). 2-Bromo-1,1-diethoxyethane (71.5 g, 363 mmol) is added and the mixture is heated to reflux for 24 hours. The cooled mixture is filtered and concentrated under reduced pressure to yield crude 2-chlorophenyl-(2,2-diethoxyethyl)sulfane as a pale pink oil (101.8 g, quantitative). A 2 L, 3-necked round-bottomed flask, fitted with a mechanical stirrer, condenser and addition funnel is charged with chlorobenzene (1 L) and polyphosphoric acid (200 g) and the mixture is heated to reflux. At reflux the crude (2-chlorophenyl)(2,2-diethoxyethyl)sulfane is added dropwise over 1.5 hours and the mixture is refluxed for a further 24 hours. The cooled organic layer is decanted and concentrated under reduced pressure. The crude material is subjected to chromatography on silica (hexane) to provide the title compound as a brown oil (54.4 g, 93% yield).

1. customA 2 L, 3-necked round-bottomed flask, fitted with a mechanical stirrer, condenser and addition funnel
2. temperaturethe mixture is heated to reflux
3. additionis added dropwise over 1.5 hours
4. temperaturethe mixture is refluxed for a further 24 hours
5. customThe cooled organic layer is decanted
6. concentrationconcentrated under reduced pressure

ORD record

ord-e31498cd1f3942cf85f78b743a4101b2

Source dataset

uspto-grants-2009_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07547691B2