HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfide → HCID 86692645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | HCID 86692646 | HCID 86692646 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86692645 | HCID 86692645 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006568B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-ae6e1c04e9394dceb7506b803d511a6c |
| Source note | uspto-grants-2015_04 |