HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350993Generated: October 25, 2026
Triphenylphosphine → HCID 60128036, compound
https://huagongshe.com/reaction/350993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-Fluoro-4-hydroxybenzonitrile | HCID 2734675 | — |
| Reactant | methyl (2S)-3-hydroxy-2-methylpropanoate | HCID 10192563 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 60128036 | HCID 60128036 | 8.1% |
Reaction Steps
To a stirred solution of 2-fluoro-4-hydroxybenzonitrile (1.0 g, 7.3 mmol), (S)-3-hydroxy-2-methyl-propionic acid methyl ester (0.8 mL, 7.3 mmol) and triphenylphosphine (2.3 g, 8.8 mmol) at room temperature, diethyl azodicarboxylate (1.4 mL, 8.8 mmol) was added dropwise. The mixture was stirred at room temperature overnight, diluted with ethyl acetate and washed successively with dilute aqueous sodium hydroxide, dilute aqueous hydrochloric acid, brine, and dried (MgSO4). Solvents were stripped in vacuo. The resulting oil was washed with diethyl ether and the precipitate was filtered off. The mother liquor was adsorbed onto silica gel and the product purified by flash column chromatography (40% ethyl acetate/hexane), affording 0.14 g of a yellow oil (8% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07183293B2 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-4c9fa0b8cba6460498c48c0c63c8ad7d |
|---|
| Source note | uspto-grants-2007_02 |
|---|