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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 555710생성일: 2026년 10월 26일

Toluene → 4-Chloro-2-(2-pyrrolidin-1-yl-ethoxy)benzonitrile

https://huagongshe.com/reaction/555710

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물1-PyrrolidineethanolHCID 76288—
반응물4-Chloro-2-fluorobenzonitrileHCID 93655—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-2-(2-pyrrolidin-1-yl-ethoxy)benzonitrileHCID 63092898—

반응 단계

A mixture of 4-chloro-2-fluoro-benzonitrile (869 mg, 5.58 mmol) and 2-pyrrolidin-1-yl-ethanol (0.80 mL, 6.70 mmol) in THF (30 mL) is treated with a 0.5 M toluene solution of KHMDS (13.4 mL, 6.7 mmol) at 0° C. After completion of the reaction at RT, the reaction mixture is quenched by H2O. EtOAc is added and the organic layer is washed with brine, dried over MgSO4. Concentration in vacuo affords the corresponding 4-chloro-2-(2-pyrrolidin-1-ylethoxy)-benzonitrile. A THF (7 mL) solution of 4-chloro-2-(2-pyrrolidin-1-yl-ethoxy)-benzonitrile is added to a suspension of LAH (293 mg, 7.71 mmol) in THF (50 mL) at 0° C. The reaction is allowed to stir for 2 h at ambient temperature and then quenched by Na2SO4.10H2O, and the product is isolated by filtration with Celite and washed with THF and dried under reduced pressure to give the title compound as oil; ES-MS: M+=255.2; HPLC: AtRet=1.22 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08053457B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-3b1205e84b074fd29d04851432cdc90a
출처 메모uspto-grants-2011_11