Trimethyl orthoformate → HCID 87090386, compound

HRID 418885Notes

Reaction equation

[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([S:9]([O-:12])(=[O:11])=[O:10])[CH:4]=1.[Na+].[CH:14](OC)(OC)OC>>[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([S:9]([O:12][CH3:14])(=[O:11])=[O:10])[CH:4]=1

Participants

Reactant 2

HCID 9005Trimethyl orthoformate

HCID 23690911HCID 23690911, compound

Product 1

HCID 87090386HCID 87090386, compound

Procedure

Next, the desalted product of sodium m-styrenesulfonate was subjected to methyl esterification with trimethyl orthoformate by following the same procedure as in Example Y-1, whereby methyl m-styrenesulfonate was obtained.

Sources & evidence

ORD record: ord-57fdcbbf6a934e7ab12e1a4ea1a87c56
Source dataset: uspto-grants-2012_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08093342B2

Reaction notes

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