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HRID 1671992作成日:2026年10月25日

p-Toluenesulfonic acid → Methyl 3,5-dihydroxy-4-methylbenzoate

https://huagongshe.com/reaction/1671992

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物3,5-Dihydroxy-4-methylbenzoic AcidHCID 2748045—
溶媒MethanolHCID 887—
生成物Methyl 3,5-dihydroxy-4-methylbenzoateHCID 11458051—

反応手順

3,5-dihydroxy-4-methylbenzoic acid (5.0 g, 29.79 mmol, 1.0 eq) and PTSA (1.13 g, 5.94 mmol, 0.2 eq) were dissolved in 50 ml of methanol, and the mixture was heated to reflux for 6 h. Methanol was evaporated. The resultant solid was washed with 10% sodium bicarbonate solution. The aqueous solution was extracted thrice with ethyl acetate. The combined organic layer was dried over sodium sulphate and evaporated under vacuum. Yield: 5.25 g (96%). 1H NMR (400 MHz, DMSO-d6): δ 1.98 (s, 3H), 3.78 (s, 3H), 6.93 (s, 2H), 9.53 (s, 2H). LCMS: (ES+) m/z=183 (M+H) Method: Column: Phenomenex Luna C18 (4.6×30) mm, 5 micron Mphase A: 10% MeOH-90% H2O-10 mM NH4OAc Mphase B: 90% MeOH-10% H2O-10 mM NH4OAc

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07994171B2
出典データセットuspto-grants-2011_08
ORD IDord-da6e8ebd0b9e4c4a8497a16d779e521c
出典メモuspto-grants-2011_08