3-Phenoxy-alpha-ethynylbenzylalcohol → alpha-ethynyl-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2-fluoroethoxy)-1-propenyl]-cyclopropane-carboxylate

HRID 1639440Notes

Reaction equation

HRID 1639440 reaction equation
[CH3:1][C:2]1([CH3:16])[CH:4](/[CH:5]=[CH:6]\[C:7](=[O:12])[O:8][CH2:9][CH2:10][F:11])[CH:3]1[C:13]([OH:15])=[O:14].[C:17]([CH:19](O)[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH:21]=1)#[CH:18]>C(Cl)(Cl)Cl>[CH3:1][C:2]1([CH3:16])[C@@H:4](/[CH:5]=[CH:6]\[C:7](=[O:12])[O:8][CH2:9][CH2:10][F:11])[C@H:3]1[C:13]([O:15][CH:19]([C:17]#[CH:18])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH:21]=1)=[O:14]

Participants

4

Reactant 2

HCID 129190923-Phenoxy-alpha-ethynylbenzylalcoholHCID 86743535HCID 86743535, compound

Product 1

HCID 86740322alpha-ethynyl-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2-fluoroethoxy)-1-propenyl]-cyclopropane-carboxylate

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

Using the procedure of Step F of Example 9, (IR, cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2-fluoroethoxy)-1-propenyl]-cyclopropane-carboxylic acid and α-ethynyl-3-phenoxy-benzyl alcohol were reacted to obtain α-ethynyl-3-phenoxy-benzyl (IR,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2-fluoroethoxy) -1-propenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20= +47° ±1.5° (c=1% in CHCl3).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-2c5320a3e91d4b76bd15edb75cb8dc66
Source dataset
uspto-grants-1989_11
Patent number
US04883806

Reaction notes

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