HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Hydroxy-4-(hydroxymethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 18942783 | HCID 18942783 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Potassium Fluoride | HCID 522689 | — |
| Product | 3-Hydroxy-4-(hydroxymethyl)benzamide | HCID 18942789 | — |
Reaction Steps
To the solution of 3-t-butyldimethylsiloxy-4-bromomethylbenzamide (Compound 7.2) (0.101 g, 0.293, mmol) in 8 mL CH3CN, KF.2H2O (0.041 g, 0.44 mmol) in 4 mL H2O was added dropwise. The mixture was then stirred at room temperature for half hour. After the solvent was removed, the residue was absorbed on 500 mg silica gel. The product was obtained by flash chromatography (ethyl acetate:ethyl alcohol=10:1, Rf=0.8) as a white solid (0.0439 g, y==90.7%). 1H NMR (CD3CN) δ4.68(s,2H), 5.95(b,1H), 6.69(b,1H), 7.23-7.26(m,3H), 7.77(b,1H); 13C NMR (CD3Cl) δ60.66, 115.13, 119.44, 128.69, 133.07, 134.94, 156.10, 203.64.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05831073 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-5cd99808902c46d4bf18841df0dfe3b1 |
| Source note | uspto-grants-1998_11 |