HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15408Erstellt: 25. Oktober 2026
Iodine → Benzo[b]thiophen-7-yl-p-tolylmethanol
https://huagongshe.com/reaction/15408
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | 4-Methylbenzaldehyde | HCID 7725 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | 7-Bromobenzo[b]thiophene | HCID 12045538 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Benzo[b]thiophen-7-yl-p-tolylmethanol | HCID 68717781 | 57% |
Reaktionsschritte
A Grignard reagent was prepared using 7-bromobenzo-[b]thiophene (1.0 g), magnesium (0.13 g), a catalytic amount of iodine and tetrahydrofuran (3 mL) according to the general method. To the Grignard reagent solution was added a solution of 4-methylbenzaldehyde (0.62 g) in tetrahydrofuran (5 mL) at 0° C. under an argon atmosphere. The reaction mixture was stirred at room temperature overnight and a saturated ammonium chloride aqueous solution was added to the mixture. The mixture was extracted with diethyl ether, and the organic layer washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on aminopropylated silica gel (eluent: tetrahydrofuran). Further purification by column chromatography on silica gel (eluent; n-hexane/ethyl acetate=6/1) gave the title compound (0.68 g) as yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732596B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-791f4186fc2a410a8b3514d9786fd950 |
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| Quellennotiz | uspto-grants-2010_06 |
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