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Water → HCID 22253670, 화합물

HRID 226195
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HRID 226195 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

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

생성물 1

HCID 22253670HCID 22253670, 화합물

시약·촉매·용매 1

HCID 6212Chloroform용매2회

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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, 0.46 mol) in 150 mL chloroform over 15 minutes. The temperature was maintained between −15 and −12° C. during the addition. The reaction mixture was then allowed to warm to room temperature and the precipitated solid was filtered. The solid was mixed with 700 mL hot toluene, and then cooled. The white solid was then filtered and dried under vacuum. A yield of 77.60 g (70%) was obtained.

후처리

  1. temperatureThe temperature was maintained between −15 and −12° C. during the addition
  2. temperatureto warm to room temperature
  3. filtrationthe precipitated solid was filtered
  4. additionThe solid was mixed with 700 mL hot toluene
  5. temperaturecooled
  6. filtrationThe white solid was then filtered
  7. customdried under vacuum
  8. customA yield of 77.60 g (70%) was obtained

출처 및 근거

ORD 기록
ord-d0fd2b590ecb48a0a9a63c1bcb0c5298
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07557177B2

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