홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Water → Carbamic acid, [1-(methoxymethyl)cyclopentyl]-, phenylmethyl ester

HRID 1293396
노트
인쇄 미리보기

반응식

HRID 1293396 반응식
[CH2:1]([O:8][C:9](=[O:18])[NH:10][C:11]1([CH2:16][OH:17])[CH2:15][CH2:14][CH2:13][CH2:12]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H+].[B-](F)(F)(F)F.[Si](C=[N+]=[N-])(C)(C)[CH3:26].O>C(Cl)Cl>[CH2:1]([O:8][C:9](=[O:18])[NH:10][C:11]1([CH2:16][O:17][CH3:26])[CH2:15][CH2:14][CH2:13][CH2:12]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 28118Tetrafluoroboric acidHCID 167693TrimethylsilyldiazomethaneHCID 11557863(1-hydroxymethyl-cyclopentyl)-carbamic Acid Benzyl Ester

생성물 1

HCID 66756538Carbamic acid, [1-(methoxymethyl)cyclopentyl]-, phenylmethyl ester

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

반응 조건

온도
0 °C

실험 절차

To a cold solution (0° C.) of (1-hydroxymethyl-cyclopentyl)-carbamic acid benzyl ester (250 mg, 1 mmol) and 48% aqueous HBF4 (0.13 mL, 1 mmol) in CH2Cl2 (4 mL) was added TMSCHN2 (2N in hexane, 2 mL, 4 mmol) via syringe. The resulting mixture was stirred, at 0° C., for ½ hour followed by the addition of water (10 mL). The aqueous mixture was extracted with CH2Cl2 (2×50 mL), and the combined organic layers were dried (sodium sulfate), filtered, concentrated and chromatographed with 30% ethyl acetate/hexane to provide the titled compound. MS (DCI) m/e 264 (M+H)+.

후처리

  1. extractionThe aqueous mixture was extracted with CH2Cl2 (2×50 mL)
  2. dry with materialthe combined organic layers were dried (sodium sulfate)
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customchromatographed with 30% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-5f9d581193bd41e1bb15ae2d7a4eb2ee
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07238724B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트