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ACIDI CARBOSSILCI e DERIVATI

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+ δ- δ+<br />

R'<br />

O<br />

C Cl R Li R'<br />

O<br />

C<br />

R<br />

+<br />

Li<br />

Cl<br />

R'<br />

O<br />

C R +<br />

δ- δ+<br />

R Li R'<br />

- O<br />

+<br />

Li<br />

C R<br />

R<br />

O<br />

R' C<br />

H 2 O, H +<br />

con cadmioorganici e cuprati organici<br />

Per fermare la reazione a chetone si devono usare:<br />

2 RMgX + CdCl 2<br />

esempio:<br />

es.:<br />

CH 3<br />

Cd<br />

O<br />

R' C Cl<br />

MgBr<br />

CdCl 2<br />

+ CH3 CH2 C<br />

Cl<br />

R<br />

+<br />

OH<br />

LiCl<br />

R' C R<br />

composti organometallici meno reattivi<br />

solo con i cloruri acilici<br />

R 2 Cd + MgCl 2 + MgX 2<br />

(R = CH 3 , alchile primario, fenile)<br />

O<br />

δ- δ+<br />

+ R CuLi 2<br />

Cd<br />

CH 3 CH 2 C<br />

O<br />

-<br />

-<br />

O<br />

R' C Cl<br />

R<br />

R<br />

O<br />

Cl CH 3 CH 2 C<br />

O<br />

R' C<br />

O<br />

O<br />

C<br />

Cl + (CH ) CuLi<br />

3 2<br />

C<br />

CH3<br />

O<br />

O<br />

H C<br />

C C<br />

Cl<br />

(CH CH ) CuLi 3 2 2<br />

H<br />

C<br />

C<br />

C<br />

CH2 CH3 CH<br />

CH2 CH3 -78°C<br />

CH CH<br />

3<br />

CH2 CH3 (feromone delle formiche)<br />

92%<br />

CH 3<br />

CH 3<br />

R<br />

22

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