HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322990Generated: October 30, 2026
2-Methylbenzaldehyde → α,α-Difluoro-β-hydroxy-2-methylbenzenepropanoic acid
https://huagongshe.com/reaction/322990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzaldehyde | HCID 10722 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | α,α-Difluoro-β-hydroxy-2-methylbenzenepropanoic acid | HCID 22010354 | 44.5% |
Reaction Steps
A solution of ethyl bromodifluoroacetate (5.6 g) and 2-methylbenzaldehyde (3 g) in THF (25 mL) is added dropwise to a refluxing suspension of activated zinc dust (2.1 g) in THF (25 mL) and refluxing continued for a further 4 hours. The reaction is allowed to cool to ambient temperature, filtered through hyflo and concentrated in vacuo to give a yellow solid. The solid is taken up in ethyl acetate (50 mL) and washed with brine which leads to the formation of a white precipitate which is filtered off then partitioned between ethyl acetate (50 mL) and 1 N HCl (50 mL). The organic phase is washed with water, dried over magnesium sulphate, filtered and concentrated in vacuo to give (RS)-2,2-difluoro-3-hydroxy-3-(2-methylphenyl)propanoic acid as a yellow solid (2.4 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211234B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-13feaa4164084c12872d0c3025d1e6f3 |
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| Source note | uspto-grants-2001_04 |
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