HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428908Generated: October 30, 2026
Dimethyl Sulfide → HCID 69554424, compound
https://huagongshe.com/reaction/428908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 69556315 | HCID 69556315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69554424 | HCID 69554424 | — |
Reaction Steps
To a solution of N-chlorosucinimide (52.3 g, 0.39 mol) in dichloromethane (1.2 l) at 0° C. was added dropwise over 20 minutes dimethylsulfide (27.9 ml, 0.38 mol). To the mixture was added dropwise over 20 minutes at 0° C. a solution of (E)-3-(3-nitrophenyl)-2-penten-1-ol (Preparation 14, 80 g, 0.39 mol) in dichloromethane (300 ml). The mixture was warmed to room temperature over 1 h, stirred at room temperature for 16 h, then partitioned between water (2 l) and dichioromethane (1 l). The layers were separated ard the orgarnc layer was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica column chromatography (2 kg), eluting with 10:1 hexane/diethyl ether. Appropriate fractions were combined and concentrated in vacuo to give the title compound as a very pale yellow oil (54 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313312B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-ce52787baa3244f8acaa79e8c2698171 |
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| Source note | uspto-grants-2001_11 |
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