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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
Reactanta FarnesolHCID 3327—
ReactantSodium ChlorideHCID 5234—
ReactantChlorosuccinimideHCID 31398—
SolventDichloromethaneHCID 6344—
SolventChlorineHCID 24526—
Product1-Chloro-3,7,11-trimethyldodeca-2,6,10-trieneHCID 407340989%

Reaction Conditions

Temperature-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05827838
Source datasetuspto-grants-1998_10
ORD IDord-635d70c0f4dc4421baad112495a628c2
Source noteuspto-grants-1998_10