반응 #315004

ord-de871c125b5e4e79b83afbb6684d650d

반응 방정식

CC(C)(C)N
tert-butylamine
O=C(O)c1ccco1
furan-2-carboxylic acid
CN(C)C=O
DMF
O=C(Cl)C(=O)Cl
oxalyl chloride
CC(C)(C)NC(=O)c1ccco1
N-tert-butylfuran-2-carboxamide

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축the clear solution was concentrated in vacuo
  2. 2
    workup.DISSOLUTIONthe resulting oil was dissolved in 75 mL THF
  3. 3
    온도cooled to 0° C
  4. 4
    농축The reaction was concentrated in vacuo
  5. 5
    기타partitioned between 1N NaOH and DCM
  6. 6
    추출The aqueous layer was extracted twice with DCM
  7. 7
    농축The combined organic layers were concentrated in vacuo

실험 절차

To a slurry of furan-2-carboxylic acid (10.0 g, 89 mmol) in 100 mL DCM at 0° C. under nitrogen was added DMF (0.069 ml, 0.89 mmol) and oxalyl chloride (9.9 ml, 112 mmol) slowly in small portions over 5 min. The reaction was allowed to warm to ambient temperature. After 3 h, the clear solution was concentrated in vacuo and the resulting oil was dissolved in 75 mL THF and cooled to 0° C. A solution of tert-butylamine (28 ml, 268 mmol) in 25 mL THF was added dropwise over 1 h. The bath was allowed to expire and the slurry was stirred over the weekend. The reaction was concentrated in vacuo and partitioned between 1N NaOH and DCM. The aqueous layer was extracted twice with DCM. The combined organic layers were concentrated in vacuo to give N-tert-butylfuran-2-carboxamide as a white solid. MS m/z=168 [M+H]+. Calc'd for C9H13NO2: 167.2.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07560551B2uspto-grants-2009_07