HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341743Generated: October 25, 2026
Dimethyl Disulfide → (2-Chloro-6-fluorophenyl)(methyl)sulfane
https://huagongshe.com/reaction/341743
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 1-Chloro-3-fluorobenzene | HCID 223087 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (2-Chloro-6-fluorophenyl)(methyl)sulfane | HCID 53633719 | 126.7% |
Reaction Steps
n-Butylithium (2.5M in hexane, 129 ml) was added to a solution of 3-fluorochlorobenzene (35 g) in dry tetrahydrofuran while maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 3 hours and dimethyl disulphide (60.65 g) was added. The mixture was allowed to warm to room temperature and stirred overnight. The mixture was evaporated to dryness and the residue was suspended in ether and washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 2-chloro-6-fluorothioanisole (60 g) as a crude yellow oil containing some dimethyl disulphide, NMR (CDCl3) 2.45(s,3H), 6.95(t,1H), 7.1-7.3(m,2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856274 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-74d29cbdb4b64b6a9fac27f6d8a4488d |
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| Source note | uspto-grants-1999_01 |
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