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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586301Generated: November 3, 2026

Potassium Chloride → HCID 57013630, compound

https://huagongshe.com/reaction/1586301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ChlorideHCID 4873—
ReactantPotassium Phosphate, DibasicHCID 24450—
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantHCID 10242642HCID 10242642—
SolventEthanolHCID 702—
ProductHCID 57013630HCID 5701363084.2%

Reaction Steps

Colletotrichum gloeosporioides is cultured according to the method of Buisson and Azerad (Tet. Lett. 27, 2631-2634 (1986), herein incorporated by reference) in one liter of a medium of glucose (30 grams), KH2PO4 (1 gram), K2HPO4 (2 grams), corn steep liquor (10 grams) MgSO4.7H2O (0.5 gram), NaNO3 (2 grams), FeSO4.7H2O (0.02 gram), and KCl (0.5 gram) with rotary shaking at 25° C. Two grams of 5-fluoro-2-carboethoxy-1-indanone is dissolved in 2 ml of 95% ethanol, the resulting solution is added to the culture, and shaking is resumed. The reaction is followed by TLC (staining with anisaldehyde) to monitor the consumption of starting material and the production of product alcohol. After approximately 48 hours the reaction is judged complete, and the reaction is terminated by removing from the shaker and adding 20-30 grams of Celite. The resulting suspension is suction filtered through a pad of Celite and the clear yellow filtrate is extracted with ethyl acetate (4×200 ml). The extracts are combined, dried over MgSO4, filtered, and rotary evaporated to leave 1.7 grams of (1S,2S)-1-hydroxy-2-carboethoxy-5-fluoroindane as a yellow oil. The chiral purity of the product is greater than 98% as judged by chiral chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05942644
Source datasetuspto-grants-1999_08
ORD IDord-4e1e851d411f400d839bc8e039266710
Source noteuspto-grants-1999_08