Hydrogen Bromide → Methyl 2-(2,6-Dipropyl-4-Bromomethyl-Phenoxy)Phenylacetate

Reaction equation

[BrH:31].[C:32]([Cl:33])([Cl:34])([Cl:35])[Cl:36].[CH2:1]([CH2:2][CH3:3])[c:4]1[c:5]([O:6][c:7]2[c:8]([CH2:13][C:14](=[O:15])[O:16][CH3:17])[cH:9][cH:10][cH:11][cH:12]2)[c:18]([CH2:24][CH2:25][CH3:26])[cH:19][c:20]([CH2:22][OH:23])[cH:21]1.[P:27]([Br:28])([Br:29])[Br:30]>>[CH2:1]([CH2:2][CH3:3])[c:4]1[c:5]([O:6][c:7]2[c:8]([CH2:13][C:14](=[O:15])[O:16][CH3:17])[cH:9][cH:10][cH:11][cH:12]2)[c:18]([CH2:24][CH2:25][CH3:26])[cH:19][c:20]([CH2:22][Br:28])[cH:21]1

Participants

Reactant 4

HCID 260Hydrogen Bromide

HCID 5943Carbon Tetrachloride

HCID 24614Phosphorus tribromide

HCID 19934855HCID 19934855, compound

Product 1

HCID 19934848Methyl 2-(2,6-Dipropyl-4-Bromomethyl-Phenoxy)Phenylacetate

Sources & evidence

ORD record: ord-e9b863ac90744be1befe0f020ad6de1b
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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