Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343878Generated: October 31, 2026

Iodine → HCID 939755, compound

https://huagongshe.com/reaction/343878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantHydrazineHCID 9321—
ReactantMethyl 3-chloro-6-methoxybenzo[b]thiophene-2-carboxylateHCID 755545—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 939755HCID 93975557%

Reaction Steps

A 100 ml, round bottomed flask, reflux condenser, gas inlet and Teflon stirrer were oven dried for 12 hours at 160° C. The apparatus was rapidly assembled, flushed with dry nitrogen gas, and cooled to room temperature. The reaction flask was charged with methyl 6-methoxy-3-chlorobenzo[b]thiophene-2-carboxylate (1.50 g, 5.85 mmole), anhydrous methanol (Aldrich, 50 ml), and anhydrous hydrazine (Aldrich, 2.5 equivalents, 0.47 g, 0.45 ml, 14.61 mmole). The stirred reaction mixture was brought to reflux and the progress of the reaction monitored by TLC (Silica, 1:1 hexane:ethyl acetate, iodine and UV visualization). After 72 hours, the completed reaction was cooled to room temperature, and further cooled to 5° C. for 1 hour. The resulting solid was filtered, washed with cold methanol (2×10 ml), and dried in vacuo. This resulted in 0.856 g of the desired material, as a white amorphous powder which was used directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05863936
Source datasetuspto-grants-1999_01
ORD IDord-c1df27f3edd645c9beaae5186e5fccd7
Source noteuspto-grants-1999_01