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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263090Generated: October 27, 2026

Tetrahydrofuran → Trans-4-hydroxy-3-phthalimidocyclopentene

https://huagongshe.com/reaction/1263090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 2-(carbonochloridoyl)benzoateHCID 11159939—
Reactanttrans-3-Amino-4-hydroxycyclopentene toluenesulfonateHCID 86737601—
SolventTriethylamineHCID 8471—
ProductTrans-4-hydroxy-3-phthalimidocyclopenteneHCID 12943979—

Reaction Steps

A 31.3 g. (0.115M) quantity of dl-trans-3-amino-4-hydroxycyclopentene toluenesulfonate is dissolved in 240 ml. of tetrahydrofuran and 47 ml. (0.46M) of triethylamine. The resultant stirred solution is cooled to 5° and treated dropwise with 22.8 g. (0.115M) of o-methoxycarbonylbenzoylchloride. The reaction is then allowed to warm to 25°. After 48 hours the reaction is partitioned between Ethyl acetate and water. The ethyl acetate layer is dried over magnesium sulfate and concentrated in vacuo leaving 29.6 g. of residue. This residue is chromatographed over silica gel 60 eluted with 5 l. of (10-90) and 7.5 l. of (20-80) acetone-methylene chloride. Three hundred ml. fractions are collected. The product is isolated in fractions 25-34, which upon standing crystallizes to yield 14.2 g. of dl-trans-4-hydroxy-3-phthalido-cyclopentene, m.p. 114°-116°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04455430
Source datasetuspto-grants-1984_06
ORD IDord-6d76454c9efc4ee6b2a10ee7729ef8c5
Source noteuspto-grants-1984_06