Can anyone help me with these cyclization questions?

CyclizationCyclization

2 Answers
Oct 2, 2016

Here are my suggestions.

Explanation:

(a) Malonate "S"_"N"2 Displacement

Malonate 1Malonate 1

(b) Malonate Conjugate "S"_"N"2 Displacement

Malonate 2Malonate 2

(c) Epoxide Ring Opening

EpoxideEpoxide

Oct 2, 2016

Question 1: probably the easiest, this is standard carbanion and enolate chemistry.

Explanation:

The substrate is:

Cl(CH_2)CH=CH(CH_2)_4OC(=O)CH_2C(=O)OMe; the methylene protons between the 2 carbonyl groups to the right are enolizable to give:

Cl(CH_2)CH=CH(CH_2)_4OC(-O^-)=CHCO_2Me.

This is the enolate, and this is the carbanion:

Cl(CH_2)CH=CH(CH_2)_4OC(=O)-C^(-)(H)CO_2Me.

This reacts as the carbanion to effect ring closure at the allylic carbon on the other end of the chain to eliminate halide.

The way it is drawn on the paper is much more intuitive than the way I have drawn it in this editor, because you can see the potential C-C bond formed between the enolizable carbon and the allylic position.

The point is that RO(O=)C-CH_2CO_2Me protons are enolizable by methoxide, and once formed this carbanion can react at the other end of the chain to form a C-C with halide eliminated.