HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226921Generated: October 30, 2026
Acetic Acid → 1,2,3,4-Tetrahydro-7-phenylmethoxycyclopent[b]indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/2226921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl 3-oxocyclopentanecarboxylate | HCID 223136 | — |
| Reactant | (4-(Benzyloxy)phenyl)hydrazine monohydrochloride | HCID 3016725 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2,3,4-Tetrahydro-7-phenylmethoxycyclopent[b]indole-2-carboxylic acid ethyl ester | HCID 54188262 | 59.9% |
Reaction Steps
To 250 ml of 80% acetic acid in water, were added 4-phenylmethoxyphenylhydrazine hydrochloride (30 g, 0.12 mole) and 3-oxocyclopentane carboxylic acid ethyl ester (20 g, 0.13 mole). After stirring at ambient temperature for one hour and then at 100° C. for four hours, the mixture was cooled and poured into one liter of water. After stirring for five minutes, the mixture was extracted with ethyl acetate (3×). The organic layer was washed successively with water (2×) and saturated sodium chloride solution, and thereafter dried over anhydrous MgSO4. After filtering, the solution was concentrated to a dark oil (~48 g), which was eluted on a silica gel column with 5% ethyl acetate/dichloromethane via HPLC. The desired fractions were combined and concentrated to give the product as a thick brown oil (24.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05350762 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-faadc4a600154045b252b522f906083a |
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| Source note | uspto-grants-1994_09 |
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