3-Phenoxybenzyl alcohol → HCID 54307763, compound

HRID 485720Notes

Reaction equation

HRID 485720 reaction equation
[CH3:1][C:2]1([CH3:12])[C@H:4]([CH:5]=[C:6]=[CH:7][Cl:8])[C@H:3]1[C:9]([OH:11])=[O:10].[O:13]([C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][CH:27]=1)[CH2:23]O)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH3:1][C:2]1([CH3:12])[C@H:4]([CH:5]=[C:6]=[CH:7][Cl:8])[C@H:3]1[C:9]([O:11][CH2:23][C:22]1[CH:25]=[CH:26][CH:27]=[C:20]([O:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:21]=1)=[O:10]

Participants

3

Reactant 2

HCID 262953-Phenoxybenzyl alcoholHCID 131714316HCID 131714316, compound

Product 1

HCID 54307763HCID 54307763, compound

Procedure

Using the procedure of Example 1, 1.2 g of the acid of Example 27 and 1 g of 3-phenoxy-benzyl alcohol were reacted to obtain 3-phenoxy-benzyl (1R,trans) 2,2-dimethyl-3-(3-chloro-1,2-propadienyl)-cyclopropane-carboxylate.

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-c3518b5bf5d147d7b7647a4ee941a46b
Source dataset
uspto-grants-1985_08
Patent number
US04537897

Reaction notes

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