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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470830Generated: November 1, 2026

Sodium Sulfide → HCID 86692645, compound

https://huagongshe.com/reaction/1470830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfideHCID 14804—
ReactantHCID 86692646HCID 86692646—
SolventMethanolHCID 887—
ProductHCID 86692645HCID 8669264575%

Reaction Steps

Compound (3) from the previous step was dissolved into 500 ml slightly boiling methanol, and a solution of sodium sulfide in 500 ml methanol was added drop-wise over about 1 hour at boiling temperature. The reactant was then kept at boiling temperature for about 1 hour. Methanol was removed by rotary evaporation and the sticky residue was absorbed by silica gel. The purification of product was performed by column chromatography using petroleum ether/ethyl acetate (30:1) as the eluent. Methyl 3-bromo-4,6-dihydrothieno[3,4-b]thiophene-2-carboxylate was obtained as colorless oil. The yield was about 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006568B2
Source datasetuspto-grants-2015_04
ORD IDord-ae6e1c04e9394dceb7506b803d511a6c
Source noteuspto-grants-2015_04