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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741871Generated: October 25, 2026

Dimethyl Sulfate → HCID 15125726, compound

https://huagongshe.com/reaction/1741871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantMethyl formateHCID 7865—
ReactantPotassium CarbonateHCID 11430—
Reactant3-PhenoxyphenolHCID 12842—
ReactantSodium hydrideHCID 24758—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantHCID 10861730HCID 10861730—
ReactantMethyl 2-(3-methoxyphenoxy)phenylacetateHCID 14620154—
Reactant(E)-methyl 2-[2-(3-hydroxyphenoxy)phenyl]-3-methoxypropenoateHCID 14620157—
ProductHCID 15125726HCID 15125726—

Reaction Steps

Methyl 2-(3-phenoxyphenoxy)phenylacetate was prepared from 3-phenoxyphenol and 2-bromobenzaldehyde by the steps described in Example 1 for the preparation of methyl 2-(3-methoxyphenoxy)phenylacetate. This was the converted into (E)-methyl 3-methoxy-2-[2-(3-phenoxyphenoxy)phenyl]propenoate [1H n.m.r (250 MHz) 3.61 (3H, s), 3.78 (3H, s), 6.68-7.35 (13H, m), 7.48 (1H, s) ppm] using sodium hydride and methyl formate, and then potassium carbonate and dimethyl sulphate, using the procedure described in Example 1 for the preparation of (E)-methyl 2-[2-(3-hydroxyphenoxy)phenyl]-3-methoxypropenoate, except that just 2 equivalents of sodium hydride were used in this case.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334748
Source datasetuspto-grants-1994_08
ORD IDord-8820373568704264ab82be3bf4bccc85
Source noteuspto-grants-1994_08