HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049890Generated: November 1, 2026
Thionyl Chloride → 1-(Chloromethyl)-2-(4-fluorophenoxy)benzene
https://huagongshe.com/reaction/2049890
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 3700253 | HCID 3700253 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(Chloromethyl)-2-(4-fluorophenoxy)benzene | HCID 20343827 | — |
Reaction Steps
8.5 g of thionyl chloride are added dropwise over a 10 minutes span to a stirring mixture of 13.0 g of 2-(4-fluorophenoxy)benzyl alcohol in 80 Ml of benzene at ambient temperature. After total addition, the reaction mixture is stirred for 16 hours before being carefully poured onto 350 ml of crushed ice containing 8 ml of sodium bicarbonate. The mixture is stirred until the ice melts. The layers separate and the benzene layer is successively washed twice with 40 ml portions of a half saturated sodium bicarbonate solution, washed twice with 40 ml portions of water, washed once with 25 ml saturated sodium chloride solution, dried and rotary evaporated to provide a clear liquid. The liquid is distilled at 106°-109° C. and 0.16 mm to provide a clear colorless liquid of 2-(4-fluorophenoxy)benzyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04198417 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-6c6c0449b69c43d5ae14c3390b7f7b19 |
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| Source note | uspto-grants-1980_04 |
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