HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68231Generated: October 29, 2026
Water → 4-{[(3-Chloro-4-hydroxyphenyl)thio]methyl}benzaldehyde
https://huagongshe.com/reaction/68231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Bromomethyl)benzaldehyde | HCID 11206421 | — |
| Reactant | 2-Chloro-4-mercaptophenol | HCID 14369743 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-{[(3-Chloro-4-hydroxyphenyl)thio]methyl}benzaldehyde | HCID 57859811 | 84% |
Reaction Steps
Triethylamine (5.0 mL, 35.9 mmol) was added dropwise to a solution of 2-chloro-4-mercaptophenol (3.60 g, 22.4 mmol) and 4-bromomethyl benzaldehyde (3.93 g, 19.7 mmol) in dioxane (150 mL) at room temperature under nitrogen. The reaction mixture was stirred at room temperature for 20 hours. Water (100 mL) was added to the reaction mixture and it was then partitioned with ethyl acetate and brine (200 mL each). The aqueous layer was re-extracted with ethyl acetate (100 mL). The combined organic layers were dried over sodium sulphate and concentrated in vacuo affording a yellow solid. This was purified by trituration with acetonitrile (5 mL/g) for 30 minutes. After filtration this afforded a light yellow solid as the pure product, 84% yield, 5.27 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822439B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-baf0fbcee31e48baaab346ce0d70e562 |
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| Source note | uspto-grants-2014_09 |
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