HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1172280Erstellt: 26. Oktober 2026
Methanesulfonic Acid → Methyl 2-(3-chloropropoxy)indole-3-carboxylate
https://huagongshe.com/reaction/1172280
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanesulfonic Acid | HCID 6395 | — |
| Edukt | Dabco | HCID 9237 | — |
| Edukt | 3-Chloro-1-propanol | HCID 12313 | — |
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | Methyl indole-3-carboxylate | HCID 589098 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 2-(3-chloropropoxy)indole-3-carboxylate | HCID 9816818 | 65% |
Reaktionsschritte
A suspension of methyl indole-3-carboxylate (5.25 g, 30.0 mmol) and DABCO (1.84 g, 16.4 mmol) in dry CH2Cl2 (25 ml) was cooled to 0° C. under argon atmosphere, treated in one portion with NCS (4.41 g, 33.0 mmol) and the mixture stirred for 10 min. The resulting solution was added to a solution of 3-chloropropan-1-ol (3.12 g, 33.0 mmol) in dry CH2Cl2 (25 ml) containing anhydrous methane sulphonic acid (0.23 ml). The resulting suspension was stirred for 30 min and then washed with 10% aqueous Na2CO3 solution (3×25 ml). The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The resulting oil was triturated with toluene (10 ml) at 0° C. for 1 h and the solid precipitate filtered, washed with a small amount of toluene and dried in vacuo to leave the product as an off-white solid (5.22 g, 65.0%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07834010B2 |
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| Quelldatensatz | uspto-grants-2010_11 |
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| ORD ID | ord-93f6e2797d2d4cc3962b64c7de0a83af |
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| Quellennotiz | uspto-grants-2010_11 |
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