HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397836Generated: October 30, 2026
Ethyl Acetate → [2-(2,4-dichlorophenoxy)phenyl]methanol
https://huagongshe.com/reaction/397836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | 2-(2,4-dichlorophenoxy)benzaldehyde | HCID 2763427 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2-(2,4-dichlorophenoxy)phenyl]methanol | HCID 2763668 | 72.7% |
Reaction Steps
Sodium borohydride (119 mg, 3.15 mmol) was added to a solution of 2-(2,4-dichlorophenoxy)benzaldehyde (600 mg, 2.25 mmol) in isopropanol (10 ml) and DCM (20 ml). The reaction mixture was stirred for 2 hours at room temperature. A 10% aqueous solution of sodium hydrogensulphate (200 ml) was added dropwise. Ethyl acetate (300 ml) was added successively. The phases were separated. The aqueous phase was extracted with ethyl acetate (100 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane 1:3 as eluent, to give 440 mg of 1-[2-(2,4-dichlorophenoxy)phenyl]methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610721B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-cf8927e643d74c7bb859e972a021e2c0 |
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| Source note | uspto-grants-2003_08 |
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