HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480926Generated: November 1, 2026
Hydrochloric Acid → HCID 18766649, compound
https://huagongshe.com/reaction/480926
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methoxyacetyl chloride | HCID 96623 | — |
| Reactant | 1-(4-nitrophenyl)cyclopentane-1-carboxylic Acid | HCID 2853078 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18766649 | HCID 18766649 | 91.6% |
Reaction Steps
13 g (20 mmol) of triphenylphosphine complex of nickel (II) chloride were added to a solution of 25.3 g (100 mmol) of 1-(4-nitrophenyl)cyclopentanoic acid in 200 ml of a 1:1 by volume mixture of methanol and tetrahydrofuran cooled in an ice bath. 10 g of sodium boronhydride were added to the cooled mixture in small portions over 10 minutes. The resulting mixture was then stirred at room temperature for 20 minutes, at the end of which time the reaction mixture was poured into 500 ml of water and the pH was then adjusted to 4 with concentrated hydrochloric acid. This caused the precipitation of crystals of 1-(4-aminophenyl)cyclopentanecarboxylic acid which were collected by filtration. 22.2 g (150 mmol) of potassium carbonate and 100 ml of tetrahydrofuran were then added to a suspension of the crystalline product in 100 ml of water which had been cooled in an ice bath, after which 9.0 ml (100 mmol) of methoxyacetyl chloride were added. After stirring the resulting mixture at the same temperature for 30 minutes, 200 ml of water were added, the mixture was washed with ether and the pH of the ether extract was then adjusted to 4 with concentrated hydrochloric acid. This mixture was allowed to stand at room temperature for 2 hours and the resulting crystals were collected by filtration to afford 25.4 g (yield 91.6%) of the desired compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653342B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-fe58362967a449a99e35c4162080a9ad |
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| Source note | uspto-grants-2003_11 |
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