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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 23171545, 화합물

HRID 2078637
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HRID 2078637 반응식
Br[CH2:2][CH2:3][O:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[S:12]([O-])([O-:15])(=[O:14])=[O:13].[Na+].[Na+].Cl>O.C(O)C>[CH2:5]([O:4][CH2:3][CH2:2][S:12]([OH:15])(=[O:14])=[O:13])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 24436Sodium SulfateHCID 73833Benzene, ((2-bromoethoxy)methyl)-

생성물 1

HCID 23171545HCID 23171545, 화합물수율 75.8%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

A mixture of [(2-bromoethoxy)methyl]benzene (6.0 g) and sodium sulfate (3.9 g) in water (12 ml) and ethanol (36 ml) was refluxed overnight. The mixture was acidified with conc. hydrochloric acid under ice-cooling. The mixture was evaporated under reduced pressure. The residue was suspended in dichloromethane/methanol (4/1) and filtered off through Celite pad. The filtrate was evaporated to give 2-(benzyloxy)ethanesulfonic acid (4.5 g).

후처리

  1. temperaturewas refluxed overnight
  2. temperaturecooling
  3. customThe mixture was evaporated under reduced pressure
  4. filtrationfiltered off through Celite pad
  5. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-9cf1a4e8899546049ca054822f929375
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928264B2

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