HCID 85722021, compound → Acetanilide
Reaction equation
CS(Cl)(=O)=[O:3].[N:6]1C=CC=[CH:8][CH:7]=1.C(=NO)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)C.N1C=CC=CC=1>>[C:7]([NH:6][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)(=[O:3])[CH3:8]Participants
3
Procedure
A 0.15 mol/L methanesulfonyl chloride/pyridine solution was sent as a first fluid from the center at a ratio of supply pressure/back pressure of 0.15 MPa/0.07 MPa, a rotation speed of 500 rpm, and a sending temperature of 25° C., and a 0.1 mol/L acetophenone oxime/pyridine solution was introduced as a second fluid into a space between the processing surfaces at 30 mL/min. The first fluid and the second fluid were mixed in a thin film fluid, and then a solution obtained after processing was discharged from the space between the processing surfaces at 58 mL/min. As a result of HPLC analysis, substantially complete conversion to acetanilide was observed.
Workup
- additionThe first fluid and the second fluid were mixed in a thin film fluid
- customa solution obtained after processing
Sources & evidence
- ORD record
- ord-0092319d7c29477a899c93d33e6423dc
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08592498B2
Reaction notes
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