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

Sulfuric Acid → 2-Bromo-4,4-dimethylpentanoic acid

HRID 1720983
노트
인쇄 미리보기

반응식

HRID 1720983 반응식
N[C@H:2]([CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.[Br-:16].[K+].N([O-])=O.[Na+]>O>[Br:16][CH:2]([CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 253877Potassium BromideHCID 69505084-Methyl-D-leucineHCID 23668193Sodium Nitrite

생성물 1

HCID 189159242-Bromo-4,4-dimethylpentanoic acid

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
0 °C

실험 절차

A solution of (R)-2-amino-4,4-dimethylpentanoic acid (950 mg, 6.55 mmol) in 2.5N aqueous sulfuric acid (13 ml, 33 mmol) was cooled to -5° C. and treated with potassium bromide (2.72 g, 22.9 mmol) in one portion. The colorless solution was treated with sodium nitrite (680 mg, 9.86 mmol) portionwise, keeping the temperature between 0° and 3° C. over a period of 25 minutes. The reaction mixture was stirred at 0° C. for one hour and at room temperature for 1.5 hours. The reaction mixture was poured into water (10 ml). The product was extracted with ether (60 ml), washed with water (20 ml) and brine (20 ml), dried (magnesium sulfate), and concentrated in vacuo to give the title product as a colorless liquid.

후처리

  1. customthe temperature between 0° and 3° C.
  2. customof 25 minutes
  3. extractionThe product was extracted with ether (60 ml)
  4. washwashed with water (20 ml) and brine (20 ml)
  5. dry with materialdried (magnesium sulfate)
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-6721c8d229ba43a59a34d2dade673432
출처 데이터셋
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05508272

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트