HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400095Generated: October 31, 2026
Dimethyl Sulfide → 1-Chloro-3,7,11-trimethyldodeca-2,6,10-triene
https://huagongshe.com/reaction/400095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | a Farnesol | HCID 3327 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Product | 1-Chloro-3,7,11-trimethyldodeca-2,6,10-triene | HCID 4073409 | 89% |
Reaction Steps
N-Chlorosuccinimide (0.66 g, 4.95 mmol) was dissolved in 20 ml of dry CH2Cl2 under a nitrogen atmosphere. The solution was cooled to -30° C. and 0.37 ml dimethyl sulphide (5 mmol) was added. The mixture was allowed to warm to 0° C. before it was cooled to -40° C. Then farnesol (1 g, 4.5 mmol) dissolved in 2.5 ml CH2 Cl2 was added dropwise to the mixture over a period of 3 minutes. The reaction mixture was warmed to 0.C in 1 h, at which temperature it was maintained for another hour. After 15 minutes of stirring at room temperature the reaction mixture was poured into a separatory funnel which contained 12.5 ml of cold saturated NaCl. The aqueous layer was extracted with two 10 ml portions of pentane. The organic layers were combined with an additional 10 ml of pentane and washed with two 5 ml portions of cold saturated NaCl. The organic layer was dried over MgSO4 and concentrated to dryness in vacuo. Compound (b) was thus obtained in a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05827838 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-635d70c0f4dc4421baad112495a628c2 |
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| Source note | uspto-grants-1998_10 |
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