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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 54366438, 화합물

HRID 1708332
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HRID 1708332 반응식
O=[C:2]1[CH2:21][NH:20][CH:19]2[CH:14]([CH2:15][CH2:16][CH2:17][CH2:18]2)[NH:13][CH2:12][C:11](=O)[NH:10][CH:9]2[CH:4]([CH2:5][CH2:6][CH2:7][CH2:8]2)[NH:3]1.O>O1CCCC1>[CH:9]12[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]1[NH:3][CH2:2][CH2:21][NH:20][CH:19]1[CH:14]([CH2:15][CH2:16][CH2:17][CH2:18]1)[NH:13][CH2:12][CH2:11][NH:10]2
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참가 물질

4

반응물 2

HCID 962WaterHCID 53848153HCID 53848153, 화합물

생성물 1

HCID 54366438HCID 54366438, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A 1M solution of BH3 in tetrahydrofuran (265 ml.) was slowly added to 10.2 g. (33.1 mmol.) of compound (A). The solution was boiled for 24 hours. Water was then added dropwise to destroy the excess BH3 and the reaction mixture was brought to dryness. The solid residue was added to 265 ml. of a 6M hydrochloric acid solution and the mixture was refluxed overnight. Hydrochloric acid was eliminated under vacuum. The residue was digested in ethanol, filtered and dissolved in water. Concentrated ammonia was added until the pH became strongly basic. The inorganic precipitate that formed was filtered off and the filtrate was extracted with methylene chloride yielding 6.3 g. of compound (B) as a white solid after elimination of the solvent.

후처리

  1. customto destroy the excess BH3 and the reaction mixture
  2. additionThe solid residue was added to 265 ml
  3. temperatureof a 6M hydrochloric acid solution and the mixture was refluxed overnight
  4. filtrationfiltered
  5. dissolutiondissolved in water
  6. additionConcentrated ammonia was added until the pH
  7. customThe inorganic precipitate that formed
  8. filtrationwas filtered off
  9. extractionthe filtrate was extracted with methylene chloride yielding 6.3 g

출처 및 근거

ORD 기록
ord-4150957ccd5545c98e5601e8f4a7fe41
출처 데이터셋
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05358704

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