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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 26431-60-7

HRID 1363288
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HRID 1363288 반응식
Br[CH2:2][C:3]1[O:4][CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.C1N2CN3CN(C2)CN1C3.Cl.[OH2:23]>>[F:9][C:8]([F:11])([F:10])[C:6]1[CH:7]=[C:3]([CH:2]=[O:23])[O:4][CH:5]=1
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참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 962Water2회HCID 4101HexamethylenetetramineHCID 218197532-(Bromomethyl)-4-(trifluoromethyl)furan

생성물 1

HCID 2181974626431-60-7

반응 조건

온도
-78 °C

실험 절차

A mixture of 2-bromomethyl-4-trifluoromethyl-furan (500 mg, 3.57 mmol), hexamethylenetetramine (HMTA) (637 mg, 4.54 mmol) and water (2.6 mL) were placed in a 50 mL pear-shaped flask equipped with a vigreaux column atop of which is attached to dry-ice condenser chilled at −78° C. The mixture was heated at reflux for 1 h, and then treated with concentrated HCl (1.7 mL). Reflux was maintained for an additional 1 h before the reaction was cooled to rt, diluted with water and extracted with DCM (4×50 mL). The combined organic extracts were washed with water, brine, dried (Na2SO4) and carefully concentrated to give 4-(trifluoromethyl)furan-2-carbaldehyde. 1H NMR (400 MHz, CDCl3) δ ppm 7.37 (m, 1H), 8.01 (m, 1H), 9.74 (d, J=0.54 Hz, 1H).

후처리

  1. customwere placed in a 50 mL pear-shaped flask
  2. customequipped with a vigreaux column atop of which
  3. customis attached to dry-ice condenser
  4. temperatureThe mixture was heated
  5. temperatureat reflux for 1 h
  6. temperatureReflux
  7. temperaturewas maintained for an additional 1 h before the reaction
  8. temperaturewas cooled to rt
  9. extractionextracted with DCM (4×50 mL)
  10. washThe combined organic extracts were washed with water, brine
  11. dry with materialdried (Na2SO4)
  12. concentrationcarefully concentrated

출처 및 근거

ORD 기록
ord-1b5155d7e58140ae88f2d87ce0f49f03
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07884124B2

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