Ethanol → 136535-21-2
Reaction equation
[ClH:1].[NH2:2][C:3]1[CH:9]=[CH:8][C:6]([OH:7])=[CH:5][C:4]=1[OH:10].[CH2:11](O)[CH3:12]>>[Cl:1][CH2:11][C:12]1[O:10][C:4]2[CH:5]=[C:6]([OH:7])[CH:8]=[CH:9][C:3]=2[N:2]=1Participants
3
Procedure
1.78 g (11.3 mmol) of said ethyl chloromethylimidate hydrochloride, 1.22 g (7.55 mmol) of 4-aminoresorcinol hydrochloride, and 20 ml of ethanol were introduced into a two-necked flask provided with a Dimroth condenser, and the mixture was refluxed with heat in argon atmosphere for a whole day and night. After completion of the reaction and cooling, the crystal was filtered and washed with hexane, then the object was vacuum dried. There was obtained 0.40 g (2.33 mmol) of 2-chloromethyl-6-hydroxybenzoxazole, and the yield of the reaction was 30.9%.
Workup
- customprovided with a Dimroth condenser
- temperaturethe mixture was refluxed
- temperaturewith heat in argon atmosphere for a whole day
- customAfter completion of the reaction
- temperaturecooling
- filtrationthe crystal was filtered
- washwashed with hexane
- customdried
Sources & evidence
- ORD record
- ord-4f36c14eca8f40098f01b43b4e09c15d
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05206149
Reaction notes
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