GB703302A - Preparation of an erythro propane diol - Google Patents

Preparation of an erythro propane diol

Info

Publication number
GB703302A
GB703302A GB8577/52A GB857752A GB703302A GB 703302 A GB703302 A GB 703302A GB 8577/52 A GB8577/52 A GB 8577/52A GB 857752 A GB857752 A GB 857752A GB 703302 A GB703302 A GB 703302A
Authority
GB
United Kingdom
Prior art keywords
effected
erythro
caustic
phthalimidoacetaldehyde
condensation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB8577/52A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Parke Davis and Co LLC
Original Assignee
Parke Davis and Co LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Parke Davis and Co LLC filed Critical Parke Davis and Co LLC
Publication of GB703302A publication Critical patent/GB703302A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide

Abstract

In the process of the parent Specification for the manufacture of DL-erythro-2-o-carboxybenzamido-1-p-nitrophenylpropane-1:3-diol, the initial step of condensing p-nitrobenzaldehyde with a -phthalimidoacetaldehyde to produce 1-(p-nitrophenyl)-1-hydroxy-2-phthalimidopropan -3-al (in the form of an addition product with a -phthalimidoacetaldehyde) is effected in the presence of a caustic alkali. The condensation may be effected by adding the caustic alkali (preferably as a 2-10N aqueous solution) to a solution of the two reactants in an organic solvent, preferably at 0-10 DEG C., the addition being desirably stopped when the temperature has risen several degrees in order to avoid the presence of excess alkali which would partially hydrolyse the phthalimido group. In examples, the condensation is effected in dioxane in the presence of: (1) and (4) caustic soda; (2) lithium hydroxide; (3) caustic potash.
GB8577/52A 1951-04-13 1952-04-03 Preparation of an erythro propane diol Expired GB703302A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR703302X 1951-04-13

Publications (1)

Publication Number Publication Date
GB703302A true GB703302A (en) 1954-02-03

Family

ID=9061190

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8577/52A Expired GB703302A (en) 1951-04-13 1952-04-03 Preparation of an erythro propane diol

Country Status (1)

Country Link
GB (1) GB703302A (en)

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