HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004495Generated: October 30, 2026
Dimethyl Sulfide → (R,E)-4-phenylthio-3-buten-2-ol
https://huagongshe.com/reaction/1004495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaborole | HCID 2734713 | — |
| Reactant | 4-(Phenylsulfanyl)but-3-en-2-one | HCID 6269152 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (R,E)-4-phenylthio-3-buten-2-ol | HCID 11019465 | — |
Reaction Steps
(E)-4-phenylthio-3-buten-2-one (178 mg, 1.0 mmol), (S)-3,3-diphenyl-1-methyltetrahydro-1H,3H-pyrrolo[1,2-c] [1,3,2] oxazaborol (28 mg, 0.1 mmol) and MS4A (Nacalai Tesque Inc., 500 mg) were dried by a vacuum pump, followed by substituting with an argon gas. Dry toluene (5 ml) and dimethylsulfide (3.0 mmol) were added thereto and, after ice cooling, a solution of borane dimethylsulfide complex in toluene (1.07M, 0.65 ml, 0.7 mmol) was dropwise added. After stirring for two hours, an aqueous saturated ammonium chloride solution was added, followed by filtering through a cotton plug. The filtrate was washed with ethyl acetate and, after separating an aqueous layer, the organic layer was washed with 2NHCl, water, an aqueous saturated sodium hydrogen carbonate solution, water and saturated brine. After drying with anhydrous magnesium sulfate, the extract containing the titled compound as a main component was obtained by concentrating under a reduced pressure. The NMR chemical shifts of the titled compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06049009 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-fb051fc5d06644d7a20177fb8b85879c |
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| Source note | uspto-grants-2000_04 |
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