HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179479Generated: November 1, 2026
Dimethylformamide → Isopropyl 3,5-difluoro-4-formylphenylcarbamate
https://huagongshe.com/reaction/1179479
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Isopropyl 3,5-difluoro-phenylcarbamate | HCID 58978077 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Isopropyl 3,5-difluoro-4-formylphenylcarbamate | HCID 58978110 | — |
Reaction Steps
n-Butyllithium (2.5M in hexane, 112 mL, 0.279 mol) was added dropwise at −78° C. to a solution of isopropyl 3,5-difluoro-phenylcarbamate (20 g, 0.093 mol) and N,N,N,N-tetramethylethylenediamine (32 mL, 0.214 mol) in 93 mL of THF, and stirred for 30 min. Dimethylformamide (10.8 mL, 0.140 mol) was then added dropwise at −78° C., stirred for 1 h, and allowed to warm to −20° C. The reaction was then quenched with saturated aqueous ammonium chloride (100 mL). The reaction mixture was extracted with ethyl acetate, the extracts washed with brine, dried (MgSO4), and concentrated. The crude product was triturated with hexane to provide the title compound. The combined hexane washings were concentrated and purified by flash column chromatography (30% ethyl acetate/hexane) to provide additional product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279494B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-3045476fa7ab4bdb901c364235bc4af1 |
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| Source note | uspto-grants-2007_10 |
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