HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652684Generated: October 26, 2026
Acetaldehyde → 6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanol
https://huagongshe.com/reaction/652684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6,7-Dichloro-1-benzothiophene-5-ol | HCID 13289997 | — |
| Reactant | Carbontetrachloride dry-ice | HCID 86602444 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanol | HCID 13477654 | — |
Reaction Steps
To a solution of 25 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene in 145 ml of dried tetrahydrofuran at -25° to -30° is added 110 ml of 2.5M n-butyllithium maintaining a temperature below -21°. After the addition, the carbon tetrachloride-dry ice bath is replaced with an ice-water bath and the mixture is stirred at 0°-5° for 4 hrs. A solution of 7.5 ml of freshly distilled acetaldehyde in 10 ml tetrahydrofuran is added dropwise. And additional 2 ml of acetaldehyde is added and the solution is stirred for 1 hr. The solution is poured onto 500 ml of a cold 5% hydrochloric acid solution and the mixture is extracted with ethyl ether. The ether extracts are washed, dried over anhydrous magnesium sulfate, filtered and solvent is removed to give a solid. Recrystallization from ethyl acetate and hexane gives 20 g of 6,7-dichloro-5-hydroxy-α-methylbenzo[b]thiophene-2-methanol, mp 173°-174°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04672138 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-fef336982d8d42d3a031895decddd8ca |
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| Source note | uspto-grants-1987_06 |
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