US 3,946,065 A · Production of cyclopentane derivatives

Abstract

Cyclopentane derivatives of the formula ##SPC1## Wherein R.sup.1 is a group of the formula --(CH.sub.2).sub.n --X in which X is a carboxyl group or its homologue, a halogen atom or a hydroxyl group and n is an integer of from 1 to 7; Y.sup.1 is a formyl group of a carboxyl group or its homologue; and Z.sup.1 is a formyl group, a carboxyl group, a hydroxymethyl group, an acetyl group, an acetoxy group, or a hydroxyl group and a process for their preparation are disclosed. The process schematically comprises the Diels-Alder reaction of a compound having the formula R.sup.1 --CH=CH--Y.sup.1 with cyclopentadiene followed by oxidation of the bicycloheptene reaction product formed into a cyclopentane derivative in which Z.sup.1 is a formyl group, a hydroxymethyl group or a carboxy group. Subsequent conversion of this cyclopentane derivative by methylation into a diacetyl cyclopentane compound followed by peroxidation and hydrolysis results in the production of a series of cyclopentane derivatives which are useful, for example, as intermediates for the production of prostaglandins.

Claims15

Dependent claims

Cyclopentane derivatives of the formula ##SPC21##

wherein n is an integer of from 1 to 7 and Z.sup.1 is selected from the group consisting of formyl, carboxyl, hydroxymethyl, and acetyl.

A process for producing a cyclopentane derivative of the formula (Ia) ##SPC25##

wherein Ac represents an acetyl group, n is an integer of from 1 to 7;
and X is a cyano or alkoxycarbonyl group, which comprises:
1. reacting a compound of the formula (III)
x--(ch.sub.2).sub.n CH=CH--CN (III)
wherein X and n are as defined above, with cyclopentadiene at 0.degree.-200.degree.C to yield a bicycloheptene derivative of the formula (II) ##SPC26##
wherein X and n are as defined above;
2. oxidizing the bicycloheptene derivative of formula II with ozone at -78.degree. to 100.degree.C to yield an ozonide of the bicycloheptene derivative of formula (II), and
3. further oxidizing the ozonide of the bicycloheptene derivative of formula II with an organic acid and hydrogen peroxide or with hydrogen peroxide alone to yield a cyclopentane derivative of the formula (Id) ##SPC27##
wherein X and n are as defined above;
4. reacting the cyclopentane derivative of formula (Id) with a member selected from the group consisting of thionyl chloride, phosgene and oxalic chloride to yield an acid halide of the formula (Ie) ##SPC28##
wherein X and n as defined above;
and
5. reacting the acid halide of the formula (Ie) with diazomethane at ambient temperature to yield a cyclopentane derivative of the formula (If) ##SPC29##
wherein X and n are as defined above;
6. reacting the cyclopentane derivative of formula (If) with aqueous hydroiodicacid to yield a cyclopentane derivative of the formula (Ig) ##SPC30##
wherein X and n are as defined above;
and
7. reacting the cyclopentane derivative of formula (Ig) with a peracid to obtain the cyclopentane derivative of formula (Ia).

15 more elements

Dependencies are inferred from the claim text.

Production of cyclopentane derivatives

Life of this patent

Production of cyclopentane derivatives

Life of this patent

Abstract

Claims15