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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722373Generated: November 2, 2026

Water → HCID 14204115, compound

https://huagongshe.com/reaction/1722373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 14204106HCID 14204106—
ReactantHCID 20028720HCID 20028720—
SolventAcetic AcidHCID 176—
ProductHCID 14204115HCID 14204115—

Reaction Conditions

Temperature75 °C

Reaction Steps

The starting material 2-(5-hydroxypent-1-yl)bicyclo[3.3.0]octan-7-one {hexahydro-4-(5-hydroxypentyl)-2(1H)-pentalenone} (0.8 g, 3.8 mmoles) is diluted with glacial acetic acid (7 ml). The reaction is stirred and heated in a 75° C. oil bath for 24 hours, after which time water (20 ml) is added and the reaction partitioned between ether. The ether layer is separated and the aqueous phase extracted again with ether (2×50 ml). The extracts and the organic phase are combined and neutralized with saturated sodium bicarbonate. The organic phase is dried over anhydrous magnesium sulfate and the remained solvent removed under vacuum leaving a pale yellow oil. The product is kugelrohred under reduced pressure leaving a clear, colorless oil (0.5 g, 2.0 mmoles).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855322
Source datasetuspto-grants-1989_08
ORD IDord-71ff3e66a9064a25ae0380a87a98dd39
Source noteuspto-grants-1989_08