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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6730Generated: October 26, 2026

Hydrochloric Acid → (6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methanamine

https://huagongshe.com/reaction/6730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
Reactant6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-oneHCID 75582—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methanamineHCID 1571859241.9%

Reaction Steps

A solution of 6-methoxy-3,4-dihydro-1H-naphthalen-2-one (176 mg, Aldrich, U.S.A.), acetic acid (0.57 mL), methylamine (2.0 M in tetrahydrofuran, 5.0 mL), and sodium cyanoborohydride (64 mg) was stirred in 5 mL methanol for 20 h. The solution was acidified to a pH<2 with concentrated hydrochloric acid, diluted with water to a volume of 50 mL, and extracted with 50 mL of dichloromethane. The aqueous phase was made basic (pH>10) by the addition of 1 M sodium hydroxide and extracted with two 50 mL aliquots of dichloromethane. The basic dichloromethane extracts were dried in vacuo to yield 80 mg of (6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084154B2
Source datasetuspto-grants-2006_08
ORD IDord-b0f2e62aef4e412897ab38669bbf8635
Source noteuspto-grants-2006_08