돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1470987생성일: 2026년 10월 26일

Borate → (1S,4S)-1,4-bis(4-chloro-3-nitrophenyl)butane-1,4-diol

https://huagongshe.com/reaction/1470987

반응식

참여 물질

역할이름HCID투입량
반응물BorateHCID 26574—
반응물Diethylaniline-boraneHCID 83312—
반응물2-Pyrrolidinemethanol, alpha,alpha-diphenyl-, (R)-HCID 7045371—
반응물1,4-Bis(4-chloro-3-nitrophenyl)butane-1,4-dioneHCID 86649099—
용매TetrahydrofuranHCID 8028—
생성물(1S,4S)-1,4-bis(4-chloro-3-nitrophenyl)butane-1,4-diolHCID 8664910999%

반응 조건

온도10 °C

반응 단계

(R)-(+)-alpha,alpha-diphenyl-2-pyrrolidinemethanol (1.08 g, 4.28 mmol) was dissolved in 70 mL of THF at ambient temperature in a dry flask under nitrogen and the timethyl borate (650 uL, 5.54 mmol) was added dropwise. The resulting solution was stirred for 1 hr. The solution was cooled in a cold bath to ˜10° C. and the N,N-diethylaniline borane (9.18 mL, 51.6 mmol) was added dropwise with some bubbling. After 15 min, this solution was transferred to an addition funnel and added dropwise to 1,4-bis(4-chloro-3-nitrophenyl)butane-1,4-dione (Example 109B) (10.0 g, 25.2 mmol) suspended in 200 mL of THF and cooled to ˜10° C. Bubbling was observed. After the addition, mixture was stirred at ambient temperature for 4 hours. The mixture was cooled in an ice bath and 30 mL MeOH was added dropwise till bubbling stopped, then the mixture was let stir at ambient temperature for 30 min. The mixture was filtered to get rid of a trace of insoluble unreacted SM. The filtrate was concentrated, poured into 1 M HCl and extracted into ethyl acetate, dried over sodium sulfate; concentrated to give the title compound (9.9 g, 99%) as a yellow waxy solid. Chiral HPLC e.e. >99.9% (RR diol was undetectable). 1H NMR (400 MHz, DMSO-d6) δ 7.94 (d, J=1.9 Hz, 2H), 7.69 (d, J=8.4 Hz, 2H), 7.60 (dd, J=8.4, 1.9 Hz, 2H), 4.65 (m, 2H), 1.62 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006387B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-417e3ce996814dc1922fd6a72b2d1e66
출처 메모uspto-grants-2015_04