Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755786Generated: November 2, 2026

Methane → (S)-5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-ylamine hydrochloride

https://huagongshe.com/reaction/1755786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant(S)-5,7-difluoro-2-[(trifluoroacetyl)amino]-1,2,3,4-tetrahydronaphthaleneHCID 15290004—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(S)-5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-ylamine hydrochlorideHCID 66789737—

Reaction Steps

Lithium hydroxide monohydrate (7.8 g, 0.2 mol) was added to a solution of (S)-5,7-difluoro-2-[(trifluoroacetyl)amino]-1,2,3,4-tetrahydronaphthalene (20.8 g, 74.5 mmol), prepared as in Example 5, in 187 mL of methanol and 21 mL of water. The mixture was stirred at reflux for 30 minutes and diluted with 200 mL of methanol. The diluted mixture then was combined with 60 mL of water, 24.8 mL of concentrated hydrochloric acid and 4.2 g of activated carbon, Darco®. The mixture was stirred for 30 minutes and then filtered through celite. The filtrate was distilled until the head temperature reached 75° C. The remaining mixture was allowed to cool and let stand for approximately 60 hours. The mixture then was cooled in an ice bath giving a crystalline material. The material was isolated by filtration and the filter residue was washed with water. Drying to constant weight in vacuo at room temperature under a nitrogen stream gave (S)-5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-ylamine hydrochloride (14.8 g, 67.6 mol), m.p. >280° C. [α]D -66.2° (c=0.162, CH3OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438150
Source datasetuspto-grants-1995_08
ORD IDord-69ffaeb546924d0e9807beeba9f71ec3
Source noteuspto-grants-1995_08