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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915968Generated: October 27, 2026

Hydrochloric Acid → (S,E)-3-Hydroxy-7-(tritylthio)hept-4-enoic acid

https://huagongshe.com/reaction/1915968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantEthyl AcetateHCID 8857—
Reactant(S,E)-3-hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)-7-(tritylthio)hept-4-en-1-oneHCID 11421639—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S,E)-3-Hydroxy-7-(tritylthio)hept-4-enoic acidHCID 1171142986%

Reaction Steps

At 0° C. to a solution of (S,E)-3-hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)-7-(tritylthio)hept-4-en-1-one (934 mg, 1.66 mmol, prepared according to the procedure in Yurek-George, A. et al, J. Am. Chem. Soc. 2004, 126, 1030) in THF (30 mL) was added a solution of LiOH (196.1 mg, 8.19 mmol) in H2O (10 mL). The reaction mixture was allowed to warm to rt over 1 h, whereupon 1M HCl was added until the pH reached 2. EtOAc (30 mL) was then added and the layers were separated. The aqueous layer was extracted with EtOAc (20 mL) the organic layers were combined, dried (MgSO4) and concentrated in vacuo. Purification by flash column chromatography (eluant 3:7-1:1-1:0 EtOAc/Hexane) gave the 6 as a white solid (600 mg, 1.43 mmol, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614193B2
Source datasetuspto-grants-2013_12
ORD IDord-7efc04afe0ca43c3adec5d122d0b2ae2
Source noteuspto-grants-2013_12