HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288723Generated: October 26, 2026
Diethyl Ether → 2-(3-Chloro-2-methylsulphenylphenyl)-4,4-dimethyloxazoline
https://huagongshe.com/reaction/1288723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | Oxazole, 2-(3-chlorophenyl)-4,5-dihydro-4,4-dimethyl- | HCID 10798476 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Chloro-2-methylsulphenylphenyl)-4,4-dimethyloxazoline | HCID 54405259 | 96.3% |
Reaction Steps
n-Butyllithium (2.5M in hexane, 4.2 ml) was added to a solution of 2-(3-chlorophenyl)-4,4-dimethyloxazoline (2 g) in THF while maintaining the temperature below -45° C. The mixture was stirred at -65° C. for 3 hours. Dimethyl disulphide (1.0 g) was added and the mixture was stirred at -65° C. for 2.5 hours and allowed to warm to room temperature. Ether was added and the mixture was washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 2-(3-chloro-2-methylsulphenylphenyl)-4,4-dimethyloxazoline (2.35 g) as a yellow oil NMR (CDCl3) 2.0(s,6H) 3.0(s,3H) 4.65(s,2H) 7.5-8.1(m,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747424 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-a654c63c60a942f981a5513281dd6080 |
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| Source note | uspto-grants-1998_05 |
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