HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Amino-4-chlorophenyl)methanol → N-(5-chloro-2-hydoxymethylphenyl)formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Amino-4-chlorophenyl)methanol | HCID 4134900 | — |
| Reactant | (Formyloxy)acetonitrile | HCID 4205685 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(5-chloro-2-hydoxymethylphenyl)formamide | HCID 12083233 | — |
Reaction Steps
A solution of 5.00 g of (2-amino-4-chlorophenyl)methanol, 2.73 g of cyanomethyl formate and 0.04 g of 4-N,N-dimethylaminopyridine in 50 ml of anhydrous tetrahydrofuran was stirred for 72 hours at 20° C. The solvent was then evaporated in vacuo and the residue was taken up in 50 ml of ethyl acetate. The solution was washed in succession twice with in each case 100 ml of 0.01 N hydrochloric acid and saturated sodium chloride solution, dried over sodium sulfate and then concentrated by evaporation in vacuo. The residue was purified by flash chromatography on silica gel with ethyl acetate/cyclohexane (2/1) as eluent. 1.41 g (24% of theory) of the title compound was thereby obtained in the form of slightly yellowish crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183274B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-80d56597d06c4e7d895c9a203c1b9c88 |
| Source note | uspto-grants-2007_02 |