반응 #69890

ord-2bf38e5f65294e9b907da17a98f437f1

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타provided 10.31 g of crude product
  2. 2
    여과followed by filtration

실험 절차

Treatment of tetrachlorophthalic anhydride (5 g, 17.49 mmol) and 4-chlororesorcinol (6.32 g, 43.73 mmol), according to the procedure described in Example 1 Step 1, provided 10.31 g of crude product. Suspension of a 9.25 g portion of this in DMF:water (1:1) followed by filtration, provided 9.70 g (2:1 DMF complex 17.16 mmol, 92.3% yield) of 2′,4,5,6,7,7′-hexachloro-3′,6′-dihydroxy-3H-spiro[isobenzofuran-1,9′-xanthen]-3-one that was isolated as an orange solid. 1H NMR (300 MHz; DMSO d6) δ 11.13 (S, 2H), 7.31 (s, 2H), 6.89 (s, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08530675B2uspto-grants-2013_09