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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074575Generated: October 31, 2026

Methyl iodide → HCID 20495945, compound

https://huagongshe.com/reaction/1074575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 13187542HCID 13187542—
ProductHCID 20495945HCID 2049594599%

Reaction Steps

By the same procedure as described in Reference Example 58, 2,3-dimethoxy-5-methyl-6-(tetrahydrofur-2-yl)-1,4-benzohydroquinone (27 g, 0.106 mole) was methylated with methyl iodide, thereby being derived into 1,2,3,4-tetramethoxy-5-methyl-6-(tetrahydrofur-2-yl)benzene (28.5 g, 98%, bp1.0 135° to 138° C.). The catalytic reduction of the compound afforded 1,2,3,4-tetramethoxy-5-methyl-6-(4-hydroxybutyl)benzene (28.2 g, 99%, oily substance).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04393075
Source datasetuspto-grants-1983_07
ORD IDord-33f482d33825431a97e9e86ebf99486b
Source noteuspto-grants-1983_07