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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 59637736, 화합물

HRID 1892017
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HRID 1892017 반응식
C([OH:4])C#C.[Br:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11](Cl)=[O:12].Cl.N1C=C[CH:18]=[CH:17][CH:16]=1>C1C=CC=CC=1>[Br:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:12][CH2:16][C:17]#[CH:18])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 7859Propargyl alcohol2회HCID 898486-Bromohexanoyl chloride

생성물 1

HCID 59637736HCID 59637736, 화합물

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

Propargyl alcohol (0.5 mL, 3.41 mmol, 1 eq.) was dissolved in 10 mL of dry pyridine and 10 mL of dry benzene under argon and this solution was cooled in an ice bath. 6-bromohexanoyl chloride (0.612 mL, 4.1 mmol, 1.2 eq.) dissolved in 10 mL of dry benzene under argon was then added dropwise to the propargyl alcohol solution and stirred overnight. The solution was acidified with 1M HCl, then extracted twice with CH2Cl2. The organic layers were twice washed with 1M NaOH, once washed with brine, and dried over Na2SO4. The solvent was removed on a rotary evaporator to yield a light brown oil.

후처리

  1. extractionextracted twice with CH2Cl2
  2. washThe organic layers were twice washed with 1M NaOH
  3. washonce washed with brine
  4. dry with materialdried over Na2SO4
  5. customThe solvent was removed on a rotary evaporator
  6. customto yield a light brown oil

출처 및 근거

ORD 기록
ord-64deded968c14208b508c33660135e30
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507572B2

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