HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254873Generated: October 30, 2026
L-Tartaric acid → HCID 86622999, compound
https://huagongshe.com/reaction/254873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | 2-(2-Methoxyphenoxy)ethyl amine | HCID 1713005 | — |
| Reactant | 4-Oxiranylmethoxy-9H-carbazole | HCID 5020710 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86622999 | HCID 86622999 | 56.9% |
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 reaction mass is raised to reflux (80° C. to 85° C.) and maintained at this temperature for 2 hour. After that, this reaction mass is added to the pre-heated (80° C. to 85° C.) solution of L(+) tartaric acid (24.32 g) (162.1 mmole) in 2-propanol (287.5 ml) and continued the reflux for next 1 hour, cooled to 50° C. to 55° C. and maintained for 1 hour. The product is filtered at the same temperature (50° C. to 55° C.) followed by three 33.5 ml wash with hot (50° C. to 55° C.) 2-Propanol. The wet product dried at 60° C. to 65° C. for 6-8 hours or till constant weight gave 33.0 g of Carvedilol tartarate (Yield 56.89%).
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-6a721eb07896482ca3f3f041478cd1f3 |
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| Source note | uspto-grants-2011_01 |
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