반응 #71017

ord-ddf7d1f4a64941a98ee522d46029ed5f

반응 방정식

N#N
N2
COC(=O)c1ccc(Cn2ncc([N+](=O)[O-])n2)o1
5-(4-nitro-[1,2,3]triazol-2-ylmethyl)-furan-2-carboxylic acid methyl ester
CC(C)[CH2][AlH][CH2]C(C)C
DiBAL
O=C([O-])[C@H](O)[C@@H](O)C(=O)[O-].[K+].[Na+]
Rochelle's salt
O=[N+]([O-])c1cnn(Cc2ccc(CO)o2)n1
title compound
O=[N+]([O-])c1cnn(Cc2ccc(CO)o2)n1
[5-(4-Nitro-[1,2,3]triazol-2-ylmethyl)-furan-2-yl]-methanol

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITfollowed by 1 h at rt
  2. 2
    workup.STIRRINGthe reaction mixture was stirred for 1 h at rt
  3. 3
    추출The aq. layer was extracted with EA (2×30 mL)
  4. 4
    건조extracts were dried over MgSO4
  5. 5
    여과filtered
  6. 6
    기타the solvents were removed under reduced pressure
  7. 7
    기타Purification of the residue by FC (50:50 hept-EA)

실험 절차

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-(4-nitro-[1,2,3]triazol-2-ylmethyl)-furan-2-carboxylic acid methyl ester (325 mg, 1.28 mmol) in THF (13.0 mL) was treated dropwise, at −10° C. with DiBAL (4.36 mL of a 1M solution in toluene, 4.36 mmol). The reaction mixture was stirred at −10° C. for 1 h followed by 1 h at rt. Sat. aq. Rochelle's salt (40 mL) was added and the reaction mixture was stirred for 1 h at rt. The aq. layer was extracted with EA (2×30 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (50:50 hept-EA) gave the title compound: TLC:rf (50:50 hept-EA)=0.28. LC-MS-conditions 02: tR=0.77 min.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08536209B2uspto-grants-2013_09