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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → Benzenemethanamine, N-butyl-2-chloro-

HRID 359980
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HRID 359980 반응식
[CH2:1]([NH:5][C:6](=O)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[Cl:13])[CH2:2][CH2:3][CH3:4].B.Cl>O1CCCC1>[CH2:1]([NH:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[Cl:13])[CH2:2][CH2:3][CH3:4]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6331BoraneHCID 347041N-butyl-2-chlorobenzamide

생성물 1

HCID 485398Benzenemethanamine, N-butyl-2-chloro-

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 21.2 g of N-(n-butyl)-2-chlorobenzamide in 100 ml of tetrahydrofuran was added with cooling to 200 ml of 1M borane in tetrahydrofuran and the mixture was stirred under reflux for 18 hours, allowed to cool, and treated with 6N hydrochloric acid. The organic solvent was evaporated, and the residue was partitioned between ether and aqueous sodium hydroxide solution. The ether layer was separated, dried, and evaporated. The residue was distilled to yield N-(n-butyl)-2-chlorobenzylamine as a colorless liquid, b.p. 65°-75° C. at 60μ.

후처리

  1. temperatureunder reflux for 18 hours
  2. temperatureto cool
  3. customThe organic solvent was evaporated
  4. customthe residue was partitioned between ether and aqueous sodium hydroxide solution
  5. customThe ether layer was separated
  6. customdried
  7. customevaporated
  8. distillationThe residue was distilled

출처 및 근거

ORD 기록
ord-b255bbb0034246bd89bf5b8e315a1036
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05003106

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