HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986247Generated: October 30, 2026
Potassium Carbonate → (2-Chlorophenyl)(2,2-diethoxyethyl)sulfane
https://huagongshe.com/reaction/1986247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | o-Chlorothiophenol | HCID 80599 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (2-Chlorophenyl)(2,2-diethoxyethyl)sulfane | HCID 59133109 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547691B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-4f219712091d42eba7f1ebf535e5becb |
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| Source note | uspto-grants-2009_06 |
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