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HRID 460214作成日:2026年10月26日

4-Hydroxybenzaldehyde → 4-(Pyrrolidin-1-ylmethyl)phenol

https://huagongshe.com/reaction/460214

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物Acetic AcidHCID 176—
反応物PyrrolidineHCID 31268—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
生成物4-(Pyrrolidin-1-ylmethyl)phenolHCID 18771978—

反応手順

To a stirred solution of 4-hydroxylbenzaldehyde (10 g, 81.9 mmol) in anhydrous CH2Cl2 (500 mL) at RT, under N2, pyrrolidine (10.2 mL, 122.9 mmol) was added, followed by NaBH(OAc)3 (34.6 g, 163.9 mmol) and AcOH (19.7 g, 327.8 mmol). After the mixture was stirred at RT for 24 h, a saturated solution of NaHCO3(aq) (150 mL) was added. The mixture was vigorously stirred for an additional 1 h and then extracted with CH2Cl2 (3×200 mL). The combined organic layer was washed with brine (300 mL), dried over MgSO4, filtered and concentrated under reduced pressure to yield the title compound as amber oil. This was used crude in the next step. MS m/z: 178 (M+1). Calc'd for C11H15NO-177.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196104B2
出典データセットuspto-grants-2007_03
ORD IDord-0e4db0ca71b5492dbedda7241f09fec1
出典メモuspto-grants-2007_03