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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586304Generated: November 2, 2026

Sucrose → HCID 57138791, compound

https://huagongshe.com/reaction/1586304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSucroseHCID 5988—
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant5-Carboxyethyl-2-carboethoxy-1-indanoneHCID 53990236—
SolventEthanolHCID 702—
ProductHCID 57138791HCID 5713879174.5%

Reaction Steps

Twenty grams of bakers' yeast (Sigma Chemical Company, type II) are suspended in an aqueous solution containing 30 grams of sucrose in a conical flask, and the mixture is placed on an orbital shaker (220 rpm) at 30° C. for 30 minutes to initiate fermentation. Two grams of 5-carboxyethyl-2-carboethoxy-1-indanone is dissolved in 2 ml of 95% ethanol, the resulting solution is added to the fermenting yeast, 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 1.5 grams of (1S,2R)-1-hydroxy-2-carboethoxy-5-carboxyethylindane as a yellowish oil (>95% enantiomeric excess as judged by chiral chromatography).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05942644
Source datasetuspto-grants-1999_08
ORD IDord-91c7aa3fe648451d90366446c8fee0fe
Source noteuspto-grants-1999_08