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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680398Generated: October 31, 2026

Methyl iodide → HCID 23456169, compound

https://huagongshe.com/reaction/1680398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantPotassium PermanganateHCID 516875—
ReactantHCID 12607167HCID 12607167—
ReactantHCID 23456200HCID 23456200—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 23456169HCID 23456169—

Reaction Steps

Following a procedure similar to that described in Example 13C, 17.48 g. (0.06 mole) of 2-phenyl-3-formyl-2,4,5,6-tetrahydro-1,4,6,6-tetrmethylcyclopenta[c]pyrrole-4-carbonitrile was oxidized with 18.9 g. (0.12 mole) of potassium permanganate in 120 ml. of pyridine and 90 ml. of water to give 4.03 g. of 2-phenyl-3-carboxy-2,4,5,6-tetrahydro-1,4,6,6tetramethylcyclopenta[c]pyrrole-4-carbonitrile which was esterified by reaction of 9.83 g. (0.032 mole) of the acid with 1.713 g. (0.035 mole) of a 50% mineral oil dispersion of sodium hydride followed by 2.23 ml. (0.036 mole) of methyl iodide. There was thus obtained 4.18 of 2-phenyl-3-carbomethoxy-2,4,5,6-tetrahydro-1,4,6,6-tetramethylcyclopenta[c]pyrrole-4-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273713
Source datasetuspto-grants-1981_06
ORD IDord-239780a188fa45d1a823e32d10b97489
Source noteuspto-grants-1981_06