HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491761Generated: November 1, 2026
Acetic Acid → 2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylamino)-2-methyl-propionic acid methyl ester
https://huagongshe.com/reaction/491761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 2-[(tert-butoxycarbonyl)amino]-2-methyl-3-oxopropanoate | HCID 22630101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylamino)-2-methyl-propionic acid methyl ester | HCID 57678923 | 53.2% |
Reaction Steps
To a solution of 2-tert-butoxycarbonylamino-2-methyl-3-oxo-propionic acid methyl ester (2.35 g, 6.71 mmol) in methanol (25 mL) was added 4-fluoroaniline (0.53 mL, 5.59 mmol) and acetic acid (0.16 mL, 2.80 mmol). A solution of sodium cyanoborohydride (188 mg, 2.99 mmol) in methanol (25 mL) was added dropwise and the reaction mixture stirred for 3 hours at room temperature post addition. The solvent was removed in vacuo and the residue dissolved in DCM (50 mL). The organic solution was treated with aqueous sodium carbonate solution (20 mL, 1N), stirred for 20 min, and the aqueous layer removed. Concentration of the organic layer followed by purification of the residue using flash chromatography (SiO2, DCM) afforded the title compound as a yellow oil (970 mg, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531565B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-d3602da0734447b5b59800747451b449 |
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| Source note | uspto-grants-2009_05 |
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