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

Water → HCID 22253670, 화합물

HRID 1072693
노트
인쇄 미리보기

반응식

HRID 1072693 반응식
[NH2:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4].[OH-].[Na+].O.[Br:11][CH:12]([CH3:16])[C:13](Br)=[O:14]>C(Cl)(Cl)Cl>[Br:11][CH:12]([CH3:16])[C:13]([NH:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4])=[O:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6119Aminoisobutyric acidHCID 14798Sodium HydroxideHCID 79047Propanoyl bromide, 2-bromo-

생성물 1

HCID 22253670HCID 22253670, 화합물수율 70.4%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

반응 조건

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
-12 °C

실험 절차

To a stirring mixture of 2-aminoisobutyric acid (52.08 g; 0.51 mol), sodium hydroxide (20.20 g; 0.51 mol), 200 mL water and 50 mL chloroform cooled to −12° C., was added a solution of 2-bromopropionyl bromide (100 g; 0.463 mol) in 150 mL chloroform. The temperature was maintained between −15 to −12° C. during the addition. The reaction mixture was then allowed to warm to room temperature and stirred for 17 hours. The precipitated solid was filtered, mixed with 700 mL hot toluene, then cooled to room temperature. The solid was filtered and dried under vacuum to afford 77.6 g (70%) of product.

후처리

  1. temperatureThe temperature was maintained between −15 to −12° C. during the addition
  2. temperatureto warm to room temperature
  3. filtrationThe precipitated solid was filtered
  4. additionmixed with 700 mL hot toluene
  5. temperaturecooled to room temperature
  6. filtrationThe solid was filtered
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-d4f22a448e564e43a9fb082e557bf200
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06911510B2

반응 노트

불러오는 중…