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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214707Generated: October 25, 2026

Hydrochloric Acid → Benzenemethanamine, 3,5-dichloro-N-methyl-, hydrochloride

https://huagongshe.com/reaction/2214707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
Reactant3,5-DichlorobenzaldehydeHCID 35746—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductBenzenemethanamine, 3,5-dichloro-N-methyl-, hydrochlorideHCID 174805193.9%

Reaction Steps

To a stirred solution of 3,5-dichlorobenzaldehyde (9.0 g, 51 mmol) in methanol (100 mL) was added methanolic methylamine (2M, 100 mL, 200 mmol) and the resulting mixture stirred for 2 h at room temperature. To this was added a solution of ZnCl2 (3.402 g, 25 mmol) slowly and NaCNBH3 (3.142 g, 50 mmol) in methanol (100 mL). After 24 h, the reaction mixture was concentrated, and the resulting residue taken up in dilute aq NaOH (0.5 N, 200 mL) and extracted with CH2Cl2 (5×50 mL). The combined CH2Cl2 extracts were dried over anhydrous Na2SO4, filtered and concentrated to give a yellow viscous liquid. The crude product was dissolved in ether (200 mL) to which was added 29 mL of 2N HCl (in ether). The resulting white 3,5-dichlorobenzyl-methylamine hydrochloride salt was filtered and dried under vacuum to give 11.20 g (97% yield) of product. 1HNMR (300 MHz, DMSO-d6) δ: 9.48 (2H, s), 7.68 (3H, s), 4.13 (2H, s), 2.50 (3H, s). MS calcd for C8H10C12N (M+H): 190.02. found: 190.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109186B2
Source datasetuspto-grants-2006_09
ORD IDord-45e53a0ec6744d269ae6ddfce2eb3329
Source noteuspto-grants-2006_09