HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272281Generated: November 1, 2026
Benzyl Bromide → 4-{[4-(Benzyloxy)phenyl]sulfanyl}-2-chlorobenzaldehyde
https://huagongshe.com/reaction/272281
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-4-fluorobenzaldehyde | HCID 145024 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-{[4-(Benzyloxy)phenyl]sulfanyl}-2-chlorobenzaldehyde | HCID 23094225 | — |
Reaction Steps
p-hydroxythiophenol (2.12 g) was dissolved in N,N-dimethylformamide (40 mL). To this solution, 2-chloro-4-fluorobenzaldehyde (2.66 g) and potassium carbonate (4.64 g) were added and the mixture was stirred for 2 hours at 50° C. Subsequently, benzyl bromide (4.00 mL) was added and the mixture was stirred for 1.5 hours at 50° C. and then for 2.5 hours at 70° C. The reaction mixture was extracted with ethyl acetate and the extract was washed sequentially with water and a saturated aqueous solution of sodium chloride. The organic phase was then dried over anhydrous sodium sulfate. Following addition of water, the solvent was removed by distillation and the residue was purified on a silica gel column chromatography (hexane:ethyl acetate=10:1). This gave the desired product as a colorless solid (5.70 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456157B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-60d4b2ccd43c4cd2a2792257e2363693 |
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| Source note | uspto-grants-2008_11 |
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