Trifluoroacetic acid → (2E)-3-{4-[bicyclo[3.3.1]non-9-ylidene(4-hydroxyphenyl)methyl]phenyl}-2-propenoic acid

To an ice-cooled solution of 44 (0.32 g, 0.755 mmol) in CH2Cl2 (4 mL) was added TFA (4 mL) slowly. The stirred reaction mixture was allowed to warm to RT over a period of 3 h. The reaction mixture was concentrated to give a yellow solid. The solid was dissolved in toluene, and the solution was concentrated to give a powder. The powder was triturated with CH2Cl2 and dried to give compound 45 as a tan powder (0.21 g, 74%). 1H NMR (400 MHz, DMSO-d6): δ 1.50-1.53 (m, 2H), 1.72 (s, 8H), 1.93-2.01 (m, 2H), 2.53-2.60 (m, 2), 6.43 (d, J=16.1 Hz, 1H), 6.66 (d, J=8.4 Hz, 2H), 6.88 (d, J=8.3 Hz, 2H), 7.09 (d, J=7.8 Hz, 2H), 7.52 (d, J=16.0 Hz, 1H), 7.57 (d, J=8.1 Hz, 2H), 9.30 (s, 1H), 12.33 (s, 1H). The compound was silated prior to EI analysis. HRMS (EI) Calcd for C31H42O3Si2: 518.2673 (M+). Found: 518.2685.

1. customThe stirred reaction mixture
2. concentrationThe reaction mixture was concentrated
3. customto give a yellow solid
4. concentrationthe solution was concentrated
5. customto give a powder
6. customThe powder was triturated with CH2Cl2
7. customdried

ORD-Eintrag

ord-b5783dffaeaf4793a8cb9f5858d6fbcd

Quelldatensatz

uspto-grants-2010_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07799828B2