Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418357Generated: October 26, 2026

Acetic Acid → 3-(Benzylamino-methyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/418357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantMethyl 3-(aminomethyl)benzoate HydrochlorideHCID 2794825—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
Product3-(Benzylamino-methyl)-benzoic acid methyl esterHCID 5919085977.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

Suspended 3-aminomethyl-benzoic acid methyl ester hydrochloride (100 mg. 0.99 mmol) in 3 mL of dichloroethane in a microwave tube and added 100 uL of AcOH. To this was added benzaldehyde (0.10 mL, 1.00 mmol). The mixture was sealed and heated at 120° C. for 20 minutes resulting in a homogeneous solution. 2 mL of MeOH was added and the mixture was treated with NaBH4 (56.8 mg, 1.50 mmol) resulting in gas evolution. The mixture stirred for 19 h. The mixture was quenched with careful addition of 5% HCl resulting in a bi-phasic mixture. The aqueous phase was removed and treated with 50×2-200 Dowex acidic ion exchange resin. The product was liberated with 10% NH3 in MeOH and concentrated to give 197 mg of 3-(benzylamino-methyl)-benzoic acid methyl ester, partially contaminated with starting benzyl amine (15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093266B2
Source datasetuspto-grants-2012_01
ORD IDord-1f7dce752bee41079aa1568231eb9191
Source noteuspto-grants-2012_01