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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731325Generated: October 26, 2026

Acetic Acid → HCID 57671205, compound

https://huagongshe.com/reaction/731325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(1S,2R)-Methyl 2-aminocyclohexanecarboxylateHCID 11008182—
SolventMethanolHCID 887—
ProductHCID 57671205HCID 57671205—

Reaction Conditions

Temperature25 °C

Reaction Steps

The crude (1S,2R)-2-amino-cyclohexanecarboxylic acid methyl ester (4.97 mmol) was dissolved in methanol (15 mL) at 25° C. and 4-fluorobenzaldehyde (0.533 mL, 4.97 mmol), glacial acetic acid (1 mL) and sodium cyanoborohydride (0.781 g, 12.4 mmol) were added sequentially. The reaction mixture was stirred at 25° C. for 19 h, and then was partitioned between saturated sodium bicarbonate solution (150 mL) and ethyl acetate (2×150 mL). The combined organic layers were dried over sodium sulfate, decanted, and were concentrated in vacuo to afford the crude product, (1S,2R)-2-(4-fluoro-benzylamino)-cyclohexanecarboxylic acid methyl ester as a yellow oil, which was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-6d1af6bfd9ce48c0b0f42668b38d96bf
Source noteuspto-grants-2009_09