Benzyl Bromide → HCID 19780666, compound

HRID 2081888Notes

Reaction equation

HRID 2081888 reaction equation
[C:1]([O:20][CH:21]1[CH2:26][CH2:25][N:24]([OH:27])[CH2:23][CH2:22]1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].C(=O)([O-])[O-].[CH2:32](Br)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>C(O)C>[C:1]([O:20][CH:21]1[CH2:26][CH2:25][N:24]([O:27][CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH2:23][CH2:22]1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

Participants

5

Reactant 3

HCID 7498Benzyl BromideHCID 19660Carbonate IonHCID 19780673HCID 19780673, compound

Product 1

HCID 19780666HCID 19780666, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The general procedure of Example 1 is repeated using 1-hydroxypiperidin-4-yl stearate, poassium carbonate and benzyl bromide in ethanol solvent to give the title compound.

Sources & evidence

ORD record
ord-865c74381091471a841adccf7e83fda1
Source dataset
uspto-grants-1993_02
Patent number
US05185448

Reaction notes

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