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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957445Generated: October 30, 2026

Methyl iodide → HCID 86745972, compound

https://huagongshe.com/reaction/1957445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86745973HCID 86745973—
ProductHCID 86745972HCID 86745972—

Reaction Steps

2-Benzyl-4-isopropyl-6-oxo-tetrahydrosaccharin of preparation 21 is reduced with sodium borohydride and methylated with methyl iodide in the presence of sodium hydride to provide 2-benzyl-4-isopropyl-6-methoxy-tetrahydrosaccharin. This is debenzylated and chloromethylated as in preparation 21 to provide 2-chloromethyl-4-isopropyl-6-methoxy-4,5,6,7-tetrahydrosaccharin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783589
Source datasetuspto-grants-1998_07
ORD IDord-116a6928ae9d47a1b880500dd94cdb4a
Source noteuspto-grants-1998_07