FR2252333A1 - Monoacylation of aromatic prim diamines - by reacting their acid addition salts with acid anhydrides in aq media - Google Patents

Monoacylation of aromatic prim diamines - by reacting their acid addition salts with acid anhydrides in aq media

Info

Publication number
FR2252333A1
FR2252333A1 FR7438776A FR7438776A FR2252333A1 FR 2252333 A1 FR2252333 A1 FR 2252333A1 FR 7438776 A FR7438776 A FR 7438776A FR 7438776 A FR7438776 A FR 7438776A FR 2252333 A1 FR2252333 A1 FR 2252333A1
Authority
FR
France
Prior art keywords
reacting
aromatic
monoacylation
prim
diamines
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.)
Granted
Application number
FR7438776A
Other languages
French (fr)
Other versions
FR2252333B1 (en
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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
Priority claimed from GB5489873A external-priority patent/GB1473659A/en
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of FR2252333A1 publication Critical patent/FR2252333A1/en
Application granted granted Critical
Publication of FR2252333B1 publication Critical patent/FR2252333B1/fr
Granted legal-status Critical Current

Links

Abstract

An aromatic primary diamine having no SO3H gps. is monoacylated by reacting a mineral acid salt of the diamine with an aliphatic acid anhydride in aq. medium. The anhydride is esp. of acetic or propionic acid and reaction is best effected in presence of 0.5-10 wt. % w.r.t. the diamine, of a surfactant. Better yields are obtd. than by reducing nitro monoacylamino cpds. Pref. diamine is m- or p-phenylenediamine.
FR7438776A 1973-11-27 1974-11-26 Monoacylation of aromatic prim diamines - by reacting their acid addition salts with acid anhydrides in aq media Granted FR2252333A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB5489873A GB1473659A (en) 1973-11-27 1973-11-27 Process for the monoacylation of aromatic diamines
GB2834474 1974-06-26

Publications (2)

Publication Number Publication Date
FR2252333A1 true FR2252333A1 (en) 1975-06-20
FR2252333B1 FR2252333B1 (en) 1978-06-16

Family

ID=26259336

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7438776A Granted FR2252333A1 (en) 1973-11-27 1974-11-26 Monoacylation of aromatic prim diamines - by reacting their acid addition salts with acid anhydrides in aq media

Country Status (5)

Country Link
JP (1) JPS5833862B2 (en)
CH (1) CH597155A5 (en)
DE (1) DE2455212C2 (en)
FR (1) FR2252333A1 (en)
IT (1) IT1030840B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3246367A1 (en) * 1982-12-15 1984-06-20 Hoechst Ag, 6230 Frankfurt METHOD FOR PRODUCING 3-ACYLAMINOANILINE

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3281467A (en) * 1964-01-20 1966-10-25 Rohm & Haas Herbicidal anilides

Also Published As

Publication number Publication date
JPS5088035A (en) 1975-07-15
FR2252333B1 (en) 1978-06-16
DE2455212C2 (en) 1984-09-13
IT1030840B (en) 1979-04-10
CH597155A5 (en) 1978-03-31
DE2455212A1 (en) 1975-05-28
JPS5833862B2 (en) 1983-07-22

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