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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112025Generated: October 25, 2026

Monobenzone → Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate

https://huagongshe.com/reaction/2112025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMonobenzoneHCID 7638—
ReactantCyanomethylenetributylphosphoraneHCID 4622928—
ReactantMethyl 2-((4-(3-hydroxypropyl)phenoxy)methyl)benzoateHCID 10780567—
SolventTolueneHCID 1140—
ProductMethyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoateHCID 6886971764.3%

Reaction Steps

Methyl 2-{[4-(3-hydroxypropyl)phenoxy]methyl}benzoate (0.50 g, 1.66 mmol) and 4-(benzyloxy)phenol (0.33 g, 1.66 mmol) was added to a dry round bottomed flask and fitted with a septum Dry toluene (10 ml) was added and N2 was flushed through the mixture for 5 minutes. (Tributylphosphoranylidene)acetonitrile (0.80 g, 3.33 mmol) was added drop wise and the reaction was performed in a single node microwave oven. After removing the solvent by evaporation the crude was purified by preparative HPLC (started with acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min)). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4). Removing the solvent by evaporation gave 0.515 gram of methyl 2-[(4-{3-[4(benzyloxy)phenoxy]-propyl}phenoxy)methyl]benzoate (yield 64.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521461B2
Source datasetuspto-grants-2009_04
ORD IDord-60cb1b3aa1c045f2bcaf6c9529fcd3ce
Source noteuspto-grants-2009_04