Hydrochloric Acid → HCID 57425852, 화합물

HRID 1727314노트

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HRID 1727314 반응식
[CH2:1]=[C:2]1[CH2:5][CH:4]([CH2:6][O:7][CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:3]1.B1C2CCCC1CCC2.[OH-:24].[Na+].OO.Cl.[NH4+].[Cl-]>O.C1COCC1>[OH:24][CH2:1][CH:2]1[CH2:5][CH:4]([CH2:6][O:7][CH2:8][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:3]1

참가 물질

9

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온도
0 °C

실험 절차

In a 10 mL flask with 1-methylene-3-benzyloxymethyl-cyclobutane (1.54 g, 8.19 mmol) inside, dry THF 11 mL was added under argon to give a colorless solution. Then cool this to 0° C., 9-BBN (0.5 M in THF, 27.4 mL, 13.7 mmol) was added drop by drop. This was allowed to warm up to ambient temperature and was left stirring for 22 hr, after which time the reaction mixture was cooled to 0° C. and H2O (0.9 mL), 3 N NaOH (2.7 mL) and 30% H2O2 (2.8 mL) were added successively. After stirring for 1 hr, 2 N HCl and saturated NH4Cl were added. The mixture was extracted with EtOAc and the separated organic phase was dried over MgSO4 and solvent evaporation gave the crude oily product, which was purified by silica gel flash chromatography (Hexane:EtOAc=3:1) to give a colorless oil (cis/trans=2/1, 1.44 g, 85%, Rf=0.16 (Hexane:EtOAc=3:1)). 1H NMR (CDCl3, 400 MHz): δ 1.52-1.60 (m), 1.86-1.90 (m), 2.12-2.19 (m), 2.36-2.64 (m), 3.39-3.41 (d, J=8), 3.49-3.51 (d, J=8), 3.54-3.56 (d, J=8), 3.64-3.66 (d, J=8), 4.51 (s), 4.53 (s), 7.2-7.4 (m). MS (FAB): expected for C13H18O2 (M+H)+ 207.28. Found 207.13807.

후처리

  1. customto give a colorless solution
  2. temperatureto warm up to ambient temperature
  3. waitwas left
  4. temperatureafter which time the reaction mixture was cooled to 0° C.
  5. stirringAfter stirring for 1 hr
  6. extractionThe mixture was extracted with EtOAc
  7. dry with materialthe separated organic phase was dried over MgSO4 and solvent evaporation
  8. customgave the crude oily product, which
  9. customwas purified by silica gel flash chromatography (Hexane:EtOAc=3:1)
  10. customto give a colorless oil (cis/trans=2/1, 1.44 g, 85%, Rf=0.16 (Hexane:EtOAc=3:1))

출처 및 근거

ORD 기록
ord-4df3589b49834623afbf76ac541b366e
출처 데이터셋
uspto-grants-2009_02
특허 번호
US07495006B2

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