Ethanol → HCID 53757515, compound
Reaction equation
C[O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH2:15][CH2:14][C@H:13]3[C@@H:8]([CH2:9][CH2:10][CH2:11][N:12]3[C:16](=[O:19])[CH2:17][CH3:18])[C:7]=2[CH:20]=1.B(Br)(Br)Br.C(O)C>C(Cl)(Cl)Cl>[OH:2][C:3]1[CH:4]=[CH:5][C:6]2[CH2:15][CH2:14][C@H:13]3[C@@H:8]([CH2:9][CH2:10][CH2:11][N:12]3[C:16](=[O:19])[CH2:17][CH3:18])[C:7]=2[CH:20]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 6.8 g of the compound obtained in Step D in 72 ml of chloroform is cooled to 0° C., then 5.3 ml of boron tribromide are added dropwise thereto. The whole is stirred for 18 hours at room temperature before the addition of 20 ml of ethanol. The resulting precipitate is filtered and washed with water, and 5.1 g of the expected compound are thereby isolated.
Workup
- filtrationThe resulting precipitate is filtered
- washwashed with water, and 5.1 g of the expected compound
- customare thereby isolated
Sources & evidence
- ORD record
- ord-4e7845b6eaba47a09a4c73aa5e6a528a
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05668142
Reaction notes
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