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

Cyclopentylamine → HCID 86729453, 화합물

HRID 1507048
노트
인쇄 미리보기

반응식

HRID 1507048 반응식
[O:1]1[CH2:3][CH:2]1[CH2:4][O:5][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH:9]=O.[CH:14]1([NH2:19])[CH2:18][CH2:17][CH2:16][CH2:15]1.[BH4-].[Na+]>CO>[O:1]1[CH2:3][CH:2]1[CH2:4][O:5][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH2:9][NH:19][CH:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2906CyclopentylamineHCID 27740493-(Oxiran-2-ylmethoxy)benzaldehydeHCID 4311764Sodium borohydride

생성물 1

HCID 86729453HCID 86729453, 화합물수율 79%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 3-(oxiran-2-ylmethoxy)benzaldehyde (1.0 g, 5.61 mmol) in MeOH (15 mL) was added cyclopentanamine (502 mg, 5.89 mmol) at room temperature. After 4 h, sodium borohydride (318 mg, 8.42 mmol) was added in portions and the mixture was stirred for another 1 h. The reaction mixture was quenched by adding aqueous 1 N HCl until the pH was adjusted to 4-5. The resulting solution was diluted with ethyl acetate, washed with water, dried over sodium sulfate, filtered and concentrated. The crude product was used in the next step without further purification. (1.1 g, yield 79%) MS (ESI+) e/z: 248.2 [M+1]+.

후처리

  1. customThe reaction mixture was quenched
  2. additionby adding aqueous 1 N HCl until the pH
  3. additionThe resulting solution was diluted with ethyl acetate
  4. washwashed with water
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude product was used in the next step without further purification

출처 및 근거

ORD 기록
ord-1af4170858c64dd39e96ace5e235c612
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221794B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트