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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060053Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 59444140, compound

https://huagongshe.com/reaction/2060053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59419744HCID 59419744—
ReactantHCID 59444053HCID 59444053—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59444140HCID 5944414056.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

1-[4-(Ethyloxy)-1-methylcyclohexyl]-4-piperidinone (D8) (0.350 g, 1.462 mmol)+ethyl (2E)-3-(2-amino-4-methylphenyl)-2-propenoate (D142) (0.1 g, 0.487 mmol) were placed in a microwave vial with 1,2-dichloroethane (DCE) (0.974 mL) and stirred for 10 mins. Sodium triacetoxyborohydride (0.387 g, 1.827 mmol) was added and the mixture heated at 140° C. for 10 mins. LCMS of the crude reaction mixture showed product (67% by u.v.). The reaction was quenched with NaHCO3 (10 mL, sat. aq) and then extracted with DCM (3×20 mL). The organic phases were combined, dried (phase sep. cartridge) and passed through a SCX-3 cartridge, eluting with DCM/MeOH to remove any neutral/acidic by-products. The product was eluted from the cartridge with 0.5 M NH3/MeOH to give a dark yellow oil. The crude product was purified by column chromatography using a 5 g cartridge and eluting with DCM-8% NH3/MeOH/DCM to give the product as a bright yellow/green oil (0.117 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278328B2
Source datasetuspto-grants-2012_10
ORD IDord-15f4712f87114b09ae726151ddf6fcd2
Source noteuspto-grants-2012_10