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

Hydrochloric Acid → 2-Fluoro-5-oxiranyl-benzenesulfonamide

HRID 990600
노트
인쇄 미리보기

반응식

HRID 990600 반응식
Br[CH2:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]([F:15])=[C:9]([S:11]([NH2:14])(=[O:13])=[O:12])[CH:10]=1)=[O:4].[BH4-].[Na+].[OH-].[Na+].Cl>CO>[F:15][C:8]1[CH:7]=[CH:6][C:5]([CH:3]2[CH2:2][O:4]2)=[CH:10][C:9]=1[S:11]([NH2:14])(=[O:13])=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 118085905-(2-Bromoacetyl)-2-fluorobenzenesulphonamide

생성물 1

HCID 109877122-Fluoro-5-oxiranyl-benzenesulfonamide수율 48.7%

시약·촉매·용매 1

HCID 887Methanol
용매

반응 조건

온도
0 °C

실험 절차

A solution of 0.5 g (1.7 mmol) of 5-bromoacetyl-2-fluoro-benzenesulfonamide V in 20 mL MeOH was cooled to 0° C. NaBH4 26 mg (0.67 mmol) was added and the reaction was stirred at 0° C. for 15 min. 4 mL of 1N NaOH was added and the reaction was stirred at 0° C. for 4 hrs. The reaction was adjusted to pH 6 by addition of dilute HCl. The volatiles were evaporated and the residue dissolved in EtOAc, washed with H2O, dried over Na2SO4 and evaporated. The product was purified by column chromatography on silica gel eluting with CH2Cl2/MeOH::9/1 to give 180 mg of VI (48%); mp 100-103° C.TLC:CH2Cl2/MeOH::9/1 single-spot material Rƒ 0.65.1H-NMR (300 MHz DMSO-D6) δ: (2.82, m, 1H), (3.14, m, 1H), (4.06, m, 1H), (7.40, t, 1H), (7.56, m, 1H), (7.66, m, 3H).

후처리

  1. stirringthe reaction was stirred at 0° C. for 4 hrs
  2. customThe volatiles were evaporated
  3. dissolutionthe residue dissolved in EtOAc
  4. washwashed with H2O
  5. dry with materialdried over Na2SO4
  6. customevaporated
  7. customThe product was purified by column chromatography on silica gel eluting with CH2Cl2/MeOH

출처 및 근거

ORD 기록
ord-7d630e878c6b4ee3b761c84695749569
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06461822B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트