HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680710Generated: October 30, 2026
Tetrahydrofuran → Trans-4-hydroxy-3-phthalimidocyclopentene
https://huagongshe.com/reaction/1680710
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | trans-4-Hydroxy-3-amino-cyclopentene | HCID 12943943 | — |
| Reactant | o-Methoxy-carbonylbenzoylchloride | HCID 86737600 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Trans-4-hydroxy-3-phthalimidocyclopentene | HCID 12943979 | — |
Reaction Steps
A quantity of dl-trans-4-hydroxy-3-amino-cyclopentene is dissolved in 450 ml. of tetrahydrofuran and 87 ml. (0.60 M) of triethylamine. The solution is cooled to 0° and treated dropwise with 59.6 g. (0.3 M) of o-methoxy-carbonylbenzoylchloride over 50 min. The reaction is then allowed to warm to 25°. After 66 hours the reaction is partitioned between ethyl acetate and water. The ethyl acetate layer is dried over magnesium sulfate and distilled in vacuo to yield 62.4 g. of residual oil. This is chromatographed over 3 kg. of silica gel 60 eluted with 6 l. of (10-90), 2.5 l. of (15-85), and 11 l. of (20-80) acetonemethylene chloride. Two hundred fifty ml. fractions are collected. The product is found in fractions 38-61. These fractions crystallized on standing to yield 25.9 g. of dl-trans-4-hydroxy-3-phthalidocyclopentene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04275214 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-89e9b783a39a486cbb6273c6d01d986f |
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| Source note | uspto-grants-1981_06 |
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