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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272129Generated: October 30, 2026

Sodium Bicarbonate → (4R,9aR)-7-hydroxymethyl-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1272129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant(4R,9aR)-7-formyl-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 86596359—
SolventMethanolHCID 887—
Product(4R,9aR)-7-hydroxymethyl-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 69358194—

Reaction Steps

To a solution of 90.0 mg (0.27 mmol) (4R,9aR)-7-formyl-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester in 1 mL methanol was added 6.2 mg (0.16 mmol) sodium borohydride. After 2 h the reaction mixture was poured into saturated aqueous sodium bicarbonate solution and extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate and filtered. The solvent was removed at a rotary evaporator and the residue was dried under high vacuum to give the compound as a light brown foam which was used without further purification (99.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208494B2
Source datasetuspto-grants-2007_04
ORD IDord-ed3dd7edd9554b41a7aceafebe672e14
Source noteuspto-grants-2007_04