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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479793생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Methyl-1-naphthol

https://huagongshe.com/reaction/1479793

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물1-Hydroxy-2-naphthaldehydeHCID 443195—
반응물Sodium borohydrideHCID 4311764—
용매WaterHCID 962—
생성물2-Methyl-1-naphtholHCID 24055—

반응 조건

온도0 °C

반응 단계

To a solution of 2-formyl-1-naphtol in tetrahydrofuran (1.0 eq, 1 mmol·mL−1) was added triethylamine (1.2 eq). The solution was cooled to 0° C. and then ethyl chloroformate (1.2 eq) was added over a period of 30 min. The solution was left under stirring during 30-60 min (white precipitates formation). The precipitates (triethylamine hydrochloride) were removed by filtration and washed with tetrahydrofuran (twice less than the amount used for the reaction). To the combined filtrates were added, at 5-15° C., an aqueous solution of NaBH4 (4.0 eq, 2.6 M). When the addition was completed, the reaction mixture was stirred at room temperature for 1-2 h, then diluted with water. The solution was cooled to 0° C. and made acidic by the slow addition of aqueous HCl (10%) (FROZING!). The aqueous solution was extracted with Et2O. The organic phases were washed with dilute solution of NaOH (10%), dried (brine, MgSO4) and concentrated in vacuo to yield methylnaphtol (usually as a solid or an oil which crystallized on standing).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409879B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-fce6c4474390408abe3dbc656c5a82d7
출처 메모uspto-grants-2016_08