HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586302Generated: October 26, 2026
Potassium Chloride → (1S,2S)-1-hydroxy-2-carboethoxy-5-methoxyindane
https://huagongshe.com/reaction/1586302
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | ethyl 5-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylate | HCID 12177975 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1S,2S)-1-hydroxy-2-carboethoxy-5-methoxyindane | HCID 57081514 | 84.3% |
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-methoxy-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-methoxyindane as a yellow oil. The chiral purity of the product is greater than 98% as judged by chiral chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05942644 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-6ce6d43c32424e5594894cf3d469a28d |
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| Source note | uspto-grants-1999_08 |
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