HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896432Generated: October 29, 2026
Chloroacetyl chloride → HCID 22350167, compound
https://huagongshe.com/reaction/896432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 5-amino-6-hydroxy-indole-2-carboxylate | HCID 22350178 | — |
| Product | HCID 22350167 | HCID 22350167 | 71.2% |
Reaction Steps
To a solution of 2.0 g (9.7 mmol) of methyl 5-amino-6-hydroxy-indole-2-carboxylate (Example 5/c) in 300 ml of tetrahydrofuran 2.45 g (29.2 mmol) of sodium hydrogencarbonate and 1.3 ml (16.3 mmol) of chloroacetyl chloride are added and the mixture is stirred at room temperature overnight. The reaction mixture is concentrated and 100 ml of water is added to the residue. The precipitated crystalls are filtered off, washed with water and suspended in 120 ml of acetonitrile. 4.05 g (29.3 mmol) of potassium carbonate is added to the suspension and the resulted mixture is stirred at room temperature overnight. The reaction mixture is concentrated and 100 ml of water is added to the residue. The product is filtered off, washed with water and dried to yield 1.7 g (71%) of the title compound. Mp.: 188-196° C. (water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919355B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-6a2c493bab2143ff84fd085047d857d6 |
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| Source note | uspto-grants-2005_07 |
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