HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949992Generated: November 1, 2026
Acetic Acid → Tert-butyl[2-(4-formylphenoxy)-1,1-dimethylethyl]carbamate
https://huagongshe.com/reaction/1949992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | tert-Butyl [2-(4-cyanophenoxy)-1,1-dimethylethyl]carbamate | HCID 57934408 | — |
| Reactant | HCID 178418950 | HCID 178418950 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl[2-(4-formylphenoxy)-1,1-dimethylethyl]carbamate | HCID 57934200 | — |
Reaction Steps
The title compound was synthesized by referring to J. Chem. Soc., 1962, 3961. To a solution of sodium hypophosphite monohydrate (1.5 g) in water (3 ml) were sequentially added tert-butyl[2-(4-cyanophenoxy)-1,1-dimethylethyl]carbamate (500 mg), pyridine (10 ml) and acetic acid (5 ml). While stirring at room temperature, Raney nickel (50% suspension in water) (2 ml) was added dropwise to the reaction mixture and the solution was stirred for 15 minutes at room temperature and for 1 hour at 40° C. After filtration through celite pad and several wash with tetrahydrofuran and methanol, the solvent was evaporated in vacuo, and the residue was neutralized by adding a saturated aqueous solution of sodium bicarbonate. After extraction with ethyl acetate, the solution was washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (443 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399520B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-aeec60278c3f409781aa82aaed5d498c |
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| Source note | uspto-grants-2013_03 |
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