HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903492Generated: October 26, 2026
Propanal → 6,7-Dichloro-5-hydroxy-alpha-ethylbenzo[b]thiophene-2-methanol
https://huagongshe.com/reaction/1903492
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propanal | HCID 527 | — |
| Reactant | 6,7-Dichloro-1-benzothiophene-5-ol | HCID 13289997 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 6,7-Dichloro-5-hydroxy-alpha-ethylbenzo[b]thiophene-2-methanol | HCID 13290045 | — |
Reaction Steps
A solution of 7.0 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene in 50 ml of dry tetrahydrofuran is cooled to -30°, using a dry ice-carbon tetrachloride bath and to the mixture is added dropwise, 35 ml of 2.2 M n-butyllithium in hexane while the temperature is maintained below -20°. Following the addition, the bath is replaced with an ice-water bath and the reaction is stirred for 4 hrs at a temperature of 0°-5°. To the mixture is added dropwise solution of 3 ml of freshly distilled proprionaldehyde in 5 ml of tetrahydrofuran. The bath is removed. The reaction mixture is stirred for 20 mins and poured onto cold 10% hydrochloric acid. The mixture is extracted 3 times with ethyl ether. The combined ether extracts are washed, dried and the solvent is removed to give a solid. Recrystallization from ethyl ether and hexane gives 5.9 g of 6,7-dichloro-5-hydroxy-α-ethylbenzo[b]thiophene-2-methanol, mp 145°-145.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436748 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-8e1f1f299d284eb0a2f183815fcfc730 |
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| Source note | uspto-grants-1984_03 |
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