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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159418Generated: November 1, 2026

Pyrrolidine → 2-Chloro-3-(1-pyrrolidinylmethyl)phenol

https://huagongshe.com/reaction/1159418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantSodium BisulfateHCID 516919—
Reactant2-Chloro-3-hydroxybenzaldehydeHCID 593376—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Chloro-3-(1-pyrrolidinylmethyl)phenolHCID 6861993895%

Reaction Steps

2-Chloro-3-hydroxybenzaldehyde (4.5 g, 0.03 mol) was added in portions for 30 min to a mixture of pyrrolidine (3. mL, 0.036 mol) and NaB(OAc)3H (7.6 g, 0.036 mol) in CH2Cl2 (50 mL) under vigorous stirring and cooling with an ice bath in an atmosphere of argon. The mixture was stirred for 3 h and cooled with an ice bath. Water (50 mL) and 5N NaHSO4 (to pH 1) were added. The organic layer was separated and discarded. The aqueous one was alkalized with saturated K2CO3 to pH 6 and extracted with chloroform (2×50 mL). The combined extracts were dried with Na2SO4, and evaporated to give the title compound (5.76 g, 95%) as white crystals. LCMS-data: (M+H)+ 214.0 and 212.0 (calculated for C11H14ClNO 211.7). 1H NMR data (DMSO-d6): 9.95 (br. s, 1H, ArOH), 7.07 (t, 1H, J1=7.8 Hz, J2=15.7, Ar—H), 6.90 (dd, 1H, J1=1.5 Hz, J2=7.6 Hz, Ar—H); 6.85 (dd, 1H, J1=1.5, J2=9.5, Ar—H), 3.63 (s, 2H, ArCH2), 2.43-2.50 (m, 4H, pyrrolidine (CH2)2N), 1.63-1.73 (m, 4H, CH2CH2CH2CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812040B2
Source datasetuspto-grants-2010_10
ORD IDord-5caaa691217d4e53b0d6bb94c98cfc6b
Source noteuspto-grants-2010_10