Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019900Generated: October 30, 2026

Acetic Acid → HCID 178501211, compound

https://huagongshe.com/reaction/1019900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178501207HCID 178501207—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
ProductHCID 178501211HCID 17850121197.2%

Reaction Steps

2,3-Dihydro-benzo[1,4]dioxine-6-carbaldehyde (198 mg, 1.21 mmol, 1.0 eq) is added at room temperature to a stirred solution of trans-4-amino-cyclohexanecarboxylic acid methyl ester (200 mg, 1.21 mmol, 1.0 eq) in 1,2-dichloroethane (8 mL) and methanol (2 mL), followed by acetic acid (80 μL, 1.39 mmol, 1.15 eq) and sodium cyanoborohydride (99 mg, 1.57 mmol, 1.3 eq). After 15 hours stirring at room temperature, the reaction mixture is extracted with dichloromethane (3×20 mL) and a saturated sodium hydrogen carbonate aqueous solution (20 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to afford trans-4-[(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-amino]-cyclohexanecarboxylic acid methyl ester as an orange oil (359 mg, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716280B2
Source datasetuspto-grants-2014_05
ORD IDord-2ad78e03d6f24a47b3a0b72ec8713f57
Source noteuspto-grants-2014_05