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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6730생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/6730

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물MethylamineHCID 6329—
반응물6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-oneHCID 75582—
반응물Sodium cyanoborohydrideHCID 5003444—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methanamineHCID 1571859241.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084154B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b0f2e62aef4e412897ab38669bbf8635
출처 메모uspto-grants-2006_08