Hydrochloric Acid → HCID 71093085, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[NH:9]C=O)[CH:5]=[CH:6][CH:7]=1.[ClH:18]>>[ClH:18].[NH2:9][CH:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:4]1[CH:3]=[C:2]([OH:1])[CH:7]=[CH:6][CH:5]=1Participants
3
Procedure
Methanol (125 mL), was cooled to 0° C., and acetyl chloride (17.8 mL) added dropwise to give a 2M solution of methanolic hydrogen chloride. N-((3-hydroxyphenyl)-(phenyl)methyl)formamide was stirred at 40° C. for 1.5 hours with the 2M methanolic hydrogen chloride. The solvent was removed under reduced pressure and the residue re-dissolved in methanol and the solvent removed under reduced pressure. This process was repeated three times to give the title compound (29.09 g, 97.9%).
Workup
- customThe solvent was removed under reduced pressure
- dissolutionthe residue re-dissolved in methanol
- customthe solvent removed under reduced pressure
Sources & evidence
- ORD record
- ord-5e94994376554191aad54f55f0983c42
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877774B2
Reaction notes
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