HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414213Generated: October 28, 2026
Iodine → 3-[2-Bromo-5-(methylsulfanyl)phenyl]propan-1-ol
https://huagongshe.com/reaction/1414213
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Bromo-2-(bromomethyl)-4-(methylsulfanyl)benzene | HCID 19437135 | — |
| Product | 3-[2-Bromo-5-(methylsulfanyl)phenyl]propan-1-ol | HCID 21486759 | — |
Reaction Steps
To a suspension of 25.0 g of magnesium ribbon in a solution of 0.5 g of iodine in 550 ml of anhydrous ether is added 5 ml of a solution of 296.0 g of 2-bromo-5-(methylthio)benzyl bromide in 250 ml of anhydrous ether. The reaction is initiated by gentle heating, and the remainder of the solution is then added dropwise so as to maintain a reflux. Subsequently, the mixture is heated and stirred under reflux for 1 hour, and then cooled to 10°. A stream of nitrogen gas that has been bubbled through a reservoir containing 48.0 g of ethylene oxide is introduced into the reaction mixture. The addition of the ethylene oxide requires two hours. The mixture is subsequently stirred as it warms to room temperature, is stirred for 4 hours at room temperature, and then hydrolyzed by pouring on a mixture of 1 kg of ice and 55.0 g of ammonium chloride. Extraction with ether, followed by conventional workup of the ether solution, yield 210.0 g of 3 -(2-bromo-5-(methylthio)phenyl)-1-propanol, bp, about 125°-127° (0.6mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001233 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-123a2dd043a446728d64381ce1a5a381 |
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| Source note | uspto-grants-1977_01 |
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