HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254871Generated: October 27, 2026
Salicylic Acid → HCID 178489624, compound
https://huagongshe.com/reaction/254871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | 2-(2-Methoxyphenoxy)ethyl amine | HCID 1713005 | — |
| Reactant | 4-Oxiranylmethoxy-9H-carbazole | HCID 5020710 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178489624 | HCID 178489624 | 70% |
Reaction Steps
A mixture of 4-(oxiran-2-ylmethoxy)-9H-carbazole (II) (25.0 g, 104.60 mmole) and 62.5 ml 2-propanol is heated to 70° C. to 80° C. To this 2-(2-methoxyphenoxy)ethylamine (III) (25.33 g, 151.67 mmole) is added in one lot. The temperature of the reaction mass is then raised to 80° C. to 82° C. and refluxed for 1 hour. The reaction mixture is added into the preheated (80° C. to 85° C.) solution of salicylic acid (18.77 g, 135.98 mmoles) in 187.5 ml of 2-propanol. The reaction mass is further refluxed for 2 hours, cooled to 50° C. to 55° C. and stirred for 1 hour at this temperature. The solid is filtered, followed by three 33 ml wash with hot (50° C. to 55° C.) 2-propanol. The wet product dried at 60° C. to 65° C. for 6 hours or till constant weight gives 39.75 g (Yield 70%) of Carvedilol salicylate, which contains about 2-2.5% of compound (IV) as an impurity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875730B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-6f2a920473da4cfb80645e85af44900e |
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| Source note | uspto-grants-2011_01 |
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