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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456683Generated: October 31, 2026

Sodium borohydride → HCID 53710797, compound

https://huagongshe.com/reaction/1456683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl 9-oxo-9H-xanthene-2-acetateHCID 12274127—
SolventEthanolHCID 702—
ProductHCID 53710797HCID 5371079743%

Reaction Steps

5.67 g (150 mmol) of sodium borohydride are added in portions to a solution of 14.2 g (50 mmol) of ethyl 9-oxo-9H-xanthene-2-acetate (Example 10d) in 130 ml of ethanol. The suspension is stirred at room temperature for 15 hours, subsequently diluted with 80 ml of ethanol and poured onto water. The product is extracted with ethyl acetate. The organic phases are washed with an aqueous saturated sodium chloride solution, combined, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. The solid residue is suspended in ethanol, the suspension is filtered and the product is dried under a high vacuum. 6.1 g (43%) of ethyl 9-hydroxy-9H-xanthene-2-acetate, melting point 214°-219° C., results as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05844024
Source datasetuspto-grants-1998_12
ORD IDord-5543cc3645bd491cbdaed7cbae0f0b1e
Source noteuspto-grants-1998_12