Reaktion #53456

Reaktionsgleichung

1-benzhydryl-3-[(4-methoxyphenyl)(methylsulfonyl)methylene]azetidine

boron tribromide

→

1-benzhydryl-3-[(4-hydroxyphenyl)(methylsulfonyl)methylene]azetidine

Ausbeute 44.3%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe residue obtained
2. 2
   Sonstigeis purified by chromatography on a silica gel column (particle size 0.04-0.06 mm, diameter 3.5 cm, height 24 cm) at a nitrogen pressure of 0.5 bar with a mixture of cyclohexane and ethyl acetate (50/50 by volume) as eluents
3. 3
   Sonstigecollecting 25 cm3 fractions
4. 4
   Einengenconcentrated to dryness under reduced pressure (2.7 kPa)
5. 5
   SonstigeThe solid obtained
6. 6
   Sonstigeis crystallized from a mixture of 30 cm3 of ethyl ether

Vorschrift

On carrying out the operation according to the procedure of Example 32 starting with 1.4 g of 1-benzhydryl-3-[(4-methoxyphenyl)(methylsulfonyl)methylene]azetidine, 10 cm3 of a 1 M boron tribromide solution and 100 cm3 of dichloromethane, the residue obtained is purified by chromatography on a silica gel column (particle size 0.04-0.06 mm, diameter 3.5 cm, height 24 cm) at a nitrogen pressure of 0.5 bar with a mixture of cyclohexane and ethyl acetate (50/50 by volume) as eluents and collecting 25 cm3 fractions. Fractions 21 to 37 are combined and concentrated to dryness under reduced pressure (2.7 kPa). The solid obtained is crystallized from a mixture of 30 cm3 of ethyl ether. 0.6 g of 1-benzhydryl-3-[(4-hydroxyphenyl)(methylsulfonyl)methylene]azetidine is obtained melting at 211° C. [NMR spectrum in DMSO-d6, T=300K, δ in ppm (300 MHz): 2.90 (3H, s, SCH3), 3.80 (2H, s, NCH2), 4.20 (2H, s, NCH2), 4.75 (1H, s, NCH), 6.80 (2H, d, J=7 Hz, 2CH arom.), between 7.10 and 7.35 (8H, m, 8CH arom.), 7.48 (4H, d, J=7 Hz, 4CH arom.), 9.80 (1H, s, OH)].

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