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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127787Generated: October 30, 2026

Tetrahydrofuran → Trans-4-hydroxy-3-phthalimidocyclopentene

https://huagongshe.com/reaction/127787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactanttrans-4-Hydroxy-3-amino-cyclopenteneHCID 12943943—
Reactanto-Methoxy-carbonylbenzoylchlorideHCID 86737600—
ProductTrans-4-hydroxy-3-phthalimidocyclopenteneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256898
Source datasetuspto-grants-1981_03
ORD IDord-2d8ee677f207477caf13f78b3a6bc973
Source noteuspto-grants-1981_03