HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437609Generated: November 2, 2026
Ethanol → 2-Chloro-5-(difluoromethoxy)phenyl-3-hydroxypropanenitrile
https://huagongshe.com/reaction/1437609
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-(2-Chloro-5-(difluoromethoxy)phenyl)ethanenitrile | HCID 57217619 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Chloro-5-(difluoromethoxy)phenyl-3-hydroxypropanenitrile | HCID 66905886 | 65% |
Reaction Steps
A 25 mL flask with a stir bar was charged with 3.0 g (13.8 mmol) of 2-(2-chloro-5-(difluoromethoxy)phenyl)ethanenitrile, 12 mL of ethanol and 1.34 mL of 37% formaldehyde solution. The mixture was stirred and a mixture of 115 μL of 40% Triton B in methanol and 38 μL of DBU was added. After a very mild exotherm, all solids dissolved. After 50 minutes at ambient temperature, the reaction was quenched by the addition of 0.5 mL of 3 N HCL. The mixture was filtered to remove floc, diluted with 2 volumes of water and extracted with butyl chloride. The extracts were water washed and stripped to an oil. This was chromatographed on 35 g of silica gel eluting with 5%→60% EtOAc in hexane to recover 2.2 g (65% yield.) of the desired product, Rf 0.18 (silica gel, EtOAc:hexane=1:4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622504B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-149d6f03d5334896aecc9bc8233de71f |
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| Source note | uspto-grants-2009_11 |
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