DEP0000326BA - Process for the preparation of monocyclic aromatic tricarbimides - Google Patents

Process for the preparation of monocyclic aromatic tricarbimides

Info

Publication number
DEP0000326BA
DEP0000326BA DEP0000326BA DE P0000326B A DEP0000326B A DE P0000326BA DE P0000326B A DEP0000326B A DE P0000326BA
Authority
DE
Germany
Prior art keywords
tricarbimides
preparation
monocyclic aromatic
hurry
els
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
Other languages
German (de)
Inventor
John Ernest Gill
John Munro
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
Publication date

Links

Description

η* A. Bohr Dr. H. Fincke Berlln-UChierlelde-Wee» Weg 28η * A. Bohr Dr. H. Fincke Berlln-UChierlelde-Wee »Route 28

KVJÜ/&925KVJÜ / & 925

is !ΛΤΠΚ'ίίis! ΛΤΠΚ'ίί

fo.fo.

i». weleher K Wasserstoff, eise äXlzyl+ öSer eine A-t ist, bei einer iiic";t u;, tc-r uai;.e££hr 91
■taster öle Abtreibung des freigi:: se taten Öi
i ». which K is hydrogen, eise ÄXlzyl + öSer an At, in a iiic ";tu;, tc-r uai; .e ££ hr 9 1
■ button oils abortion of the release :: se deeds oil

Bedingungen dergeetei:.. t, bis ftie SiloanConditions dergeetei: .. t until ftie Siloan

XiegXieg

l;s£ inerte flüofetigc ?erüii
weise mas aefe «yfeiite.rien u'rodOufct -üT
l; s £ inert flüofetigc? erüii
wise mas aefe «yfeiite.rien u'rodOufct -üT

iss ist su. beasiitea^ asß bei ö.er l^retallaag i<i«r issu Dniütisch ^b iritSirfelsiide für des Aassclilui -roa ψοί cor uui^ioncaiiooh^Aai.. ^t sorgt τ er-'cn soll«iss is su. beasiitea ^ asß bei ö.er l ^ retallaag i <i «r issu Dniütisch ^ b iritSirfelsiide für des Aassclilui -roa ψοί cor uui ^ ioncaiiooh ^ Aai .. ^ t cares τ er-'cn shall«

•Sie xi&eft -icr vorii^ ο;;^ελ Jrt'i«'.• You xi & eft -icr vorii ^ ο ;; ^ ελ Jrt'i «'.

persttir fest vtn-i sleÄe^ Ijsi ::.b<ir 2C;'-° 3 lle^c-näezi '.-SI© kSaneii unter rmr geiziger ^ei-setsiang bei vcrßiiidertsffi Bmcfe iestilliert.- utn6 eaf cli&se ^cise oder aasb ütircii iiütepletcllleö«. -tion lierßiBigt weriSeu.» de sie in fi.&n ^ewöhriiicccji !»©rtes. orgs-persttir fest vtn-i sleÄe ^ Ijsi ::. b <ir 2C ; '- ° 3 lle ^ c-Naezi'.-SI © kSaneii unter rmr stingy ^ ei-setsiang at vcrßiiidertsffi Bmcfe iestilliert .-- utn6 eaf cli & se ^ cise or aasb ütircii iiütepletcllleö «. -tion is not allowed. " de them in fi. & n ^ ewöhriiicccji! »© rtes. orgs-

ir&rlltäft ia litüfeiii uster iaeii der Ajair & rlltäft ia litüfeiii uster iaeii der Aja

In. liea ^er^emd-etsa or^t^iRcri©}': r-roli^ -^gEitü&2ü slcl-.t luslioh "elnd· -ii*a loll er.c ^ ^ -ler ~£&lcti.en wird η' »-In. liea ^ er ^ emd-etsa or ^ t ^ iRcri ©} ': r-roli ^ - ^ gEitü & 2ü slcl-.t luslioh "elnd · -ii * a loll er.c ^ ^ -ler ~ £ & lcti.en will η '»-

&Qthw&& zuglrlsh mit .Jes ΐ.*ιο'α££η ant«ratatst wsr^isa hti-;ru.-.ig -.er äbscheiuUÄ«;: des ^ & Qthw && zuglrlsh with .Jes ΐ. * Ιο'α ££ η ant «ratatst wsr ^ isa hti-; ru .-. Ig -.er äbscheiuUÄ« ;: des ^

VJS& lr©2it?r VJS & lr © 2it? R

feines iSl"fine iSl "

n%£3i-n% £ 3-

iroers"t€ij..e7Lfe£. r.:ic epas&rfeiroers "t € ij..e7Lfe £. r.:ic epas & rfe

&tics. xml· tensi s, 1.& tics. xml tensi s, 1.

flcr irorlie^c-tfeflcr irorlie ^ c-tfe

tic rtejl-srea slit i si* ..ai-ser mater Γ;11£tic rtejl-srea slit i si * ..ai-ser mater Γ; £ 11

sit ämtwlük aStr sit ämtwlük aStr

iasttri* LiI-iasttri * LiI-

IScssr* ei« ©eiIScssr * ei «© ei

ISIS

tem sic istem sic is

ie «lie Is deeie «lie is dee

is-is-

ilt &&|»:ί.ί><ϊ&«& b±&£ilt && | »: ί.ί> <ϊ &« & b ± & £

el tel t

te 5?eile igte 5? in a hurry

95s S Is fCK3 bliest95 s S Is fCK3 is blowing

cl sü£pcr,öiert tnf- ©incl sü £ pcr, öiert tnf- © in

£ gleitet» iflhrca? :i;l£ slides »iflhrca? : i; l

sfe^efSisrt* lias r.israest^lösfe ^ efSisrt * lias r.israest ^ lö

txsrmit, ·ΐtxsrmit, · ΐ

itje^f^Is unter rcritje ^ f ^ Is under rcr

£le Ä_o®bsat€ ia^efSfcr 6^# vies Theorie£ le Ä_o®bsat € ia ^ efSfcr 6 ^ # vies theory

ErirtslleErirtslle

ei 132* Z ei 132 * Z

bei 132at 132

isis

Bt% iss: els. tTssS'i^iBLS tsee. Bt% eat: els. tTssS'i ^ iBLS tsee.

fel gfel g

7*e&epiatl 17 * e & epiatl 1

«irvl «teer soff"Irvl" drank tar

e «j?te «j? t

Tf5.Ä m,T& an StallsT f 5.Ä m, T & an stalls

feeiia ^feeiia ^

1st1st

is deris that

la a2-feohöl*· tsnflla a2-feohöl * tsnfl

3. 33. 3

t be^titstasit be ^ titstasi

4949

4a4a

la. 4er to »INtiapiel 1 leip«la. 4 to "INtiapiel 1 leip"

hergg»1»3JL"thergg »1» 3JL "t

exit öeei u G lass*exit öeei u G lass *

* 2 »4* 2 »4

t 6-2t 6-2

lala

βε.*: eisβε. * : ice

a ia die S isgeloit^t, *a ia die S isgeloit ^ t, *

IC>3# S fc2*JsS.tst imd ssf tl&ser fIC> 3 # S fc2 * JsS.tst imd ssf tl & ser f

txatertxater

41βο«ε; Sei-crsiKi soll die S'a 2 ö41βο «ε; Sei-crsiKi is supposed to be the S'a 2 ö

langlong

«das··"that··

des· ia H^i C des · ia H ^ i C

lele

ei t pie! 5ei t pie! 5

lsi. eisa iuspeusioft tos. 9f6 Teiler* £,4>6-£riai l*eiisol-1ia?ih3rüroahlori<i is. 4fK* ieiltes E o^elil \i ete. ^&osseastr^a "»ei ötnejr I empor:-· tar Tors. 4Ss ü&iäss, Iö5 — € tire! Stua&ea lsag ©ingelöltet, in weloher Seit sie feste lsi. eisa iuspeusioft tos. 9 f 6 divisors * £, 4 > 6- £ riai l * eiisol-1ia? Ih3rüroahlori <i is. 4fK * ieiltes E o ^ elil \ i ete. ^ & osseastr ^ a "» ei ötnejr I upwards: - · tar Tors. 4Ss ü & iäss, Iö5 - € tire! Stua & ea lsag © ingelöltet, in which since she was fixed

lioh in 1*Κΐ*&ιιπ ge:t°Xi,ßert ist« 5er1 "SilorwKS aas ilonoohlor^Q&ol weroea sbgetriefccsa m€ üer· liil Töei fies Terlieri.cl^eralmi Τ,«1ορ1ε1β"Λ destilliertlioh in 1 * Κΐ * & ιιπ ge : t ° Xi, ßert is «5er 1 " SilorwKS aas ilonoohlor ^ Q & ol weroea sbgetriefccsa m € üer · liil Töei fies Terlieri.cl ^ eralmi Τ, «1ορ1ε1β" Λ distilled

i als i'i as i '

Beispl«!Beispl «!

it, «oarasit, «oaras

i/er £Zut:yi / er £ allotment: y

* 5 ,* 5,

©iw^© iw ^

^t aa*iu^ t aa * iu

fi© tfi © t

diethe

53 ·753 7

55*655 * 6

52.7452.74

42,642.6

1.51.5

4 «54 «5

für CL i^S-ti« i; D1 3 3 for CL i ^ S-ti « i ; D 1 3 3

firfir

tr I1S^e than..tr I 1 S ^ e than ..

t für G4. IL «-*..-Ct for G 4 . IL «- * ..- C

henkel««? v 4- s δ—tr i#iar biai 55·8handle""? v 4- s δ-tr i # iar biai 55 · 8

54 »454 »4

■6*3■ 6 * 3

5.295.29

45·. 45.545 ·. 45.5

57»δ .57-73 3.S57 »δ .57-73 3.S

IS, 3IS, 3

ta Jf 1ta Jf 1

4 r4 r

^i*^ i *

C*C *

«!, 4 y β- triiE- e trum«!, 4 y β- triiE- e trum

für 2.. ^for 2 .. ^

47? 1 46.147? 1 46.1

51· 951 9

SS.

M $9.f M $ 9.f

Claims (1)

la iela ie rriifcsrbifciten, €odttr&h cfc&ersaBcIii^ne-fcf &iiS in ©is©rriifcsrbifciten, € odttr & h cfc & ersaBcIii ^ ne-fcf & iiS in © is © its, *v±slc& iiier«s2i or^oaiscnet £13*eh timers Verdiäaawi ilrihy^roo4iloria einer prSmllres aroriatlco!i€®jits, * v ± slc & iiier «s2i or ^ oaiscnet £ 13 * eh timers Verdiäaawi i l rihy ^ roo4iloria a prSmllres aroriatlco! i € ®j V*V * ti -f*·! "»"■ £ί Λη fti -f * · ! "» "■ £ ί Λη f diethe *J.kyi-oii©r els,© n * J.kyi-oii © r els, © n & eile τ:ϋΐι& hurry τ : ϋΐι I'rJUfc&rfeiisi&eB voilen^et is»-I'rJUfc & rfeiisi & eB voilen ^ et is »- t*
2* ftrfafees. aasa /asa3>racüi I5 dadurch ^ök
t *
2 * ftrfafees. aasa / asa3> racüi I 5 thereby ^ ec
t-,tetio:istGsptirfett2T siisÄes 9t tm& 15C° Z liegt.t-, tetio: istGspt i rfett2T siisÄes 9t tm & 15C ° Z lies. 3 Vcrfu1 ^«ή1£^Γ^8ΐί-4--^Γ^£ίτ--&^^ 3 Vcrfu 1 ^ «ή1 £ ^ Γ ^ 8ΐί-4 - ^ Γ ^ £ ί ~ £ τ - & ^^ fsräjfsräj '.-el'.-el fturohfturoh eileHurry e « ausgeh I esI go out ts^'~^ts ^ '~ ^ mm L£§sa&&@& ία g timft inerten mm L £ §sa && @ & ία g timft inert 3-4®3-4® aaeh len 1 felsaaeh len 1 rock flusstiriver list«.list «.

Family

ID=

Similar Documents

Publication Publication Date Title
Wang et al. Selective monolithiation of 2, 5-dibromopyridine with butyllithium
Merker et al. Grignard Reactions of Polyhalocarbons. I. In Situ Grignard Reactions of 1, 1-Dihalides and 1, 1, 1-Trihalides with Organochlorosilanes
DEP0000326BA (en) Process for the preparation of monocyclic aromatic tricarbimides
Tureček Proton affinity of dimethyl sulfoxide and relative stabilities of C 2 H 6 OS molecules and C 2 H 7 OS+ ions. A comparative G2 (MP2) ab initio and density functional theory study
Sun et al. On-surface synthesis on nonmetallic substrates
DE1669947C3 (en) Manufacture of composites
He et al. Pummerer chemistry of benzothiophene S-oxides: Metal-free alkylation and arylation of benzothiophenes
DE893198C (en) Process for the preparation of organohalosilanes
DE2152286B2 (en) Silyl peracyl compounds and their use
DE635396C (en) Process for the production of vinyl sulfoxides and vinyl sulfones
DE102012212007A1 (en) Process for the preparation of organopolysiloxanes
Nishikida et al. ESR spectrum and structure of BrF6
US707235A (en) Mop-wringer.
DE825937C (en) Process for anodic glazing of objects made of aluminum and aluminum alloys
Ramasamy et al. Tellurium Heterocycles, I Synthesis of 2, 3-Dihydrotellurolo (2, 3-b) quinolines
DE1085877B (en) Process for the preparation of dibenzylbenzenes
CH127702A (en) Process for the preparation of a ring ketone of the aromatic series.
DE2024604C (en)
US357013A (en) Churn
DE1734177U (en) FOLDING BOX.
Martin et al. Tautomerism and chemical properties of β-oxonitrones
CH127701A (en) Process for the preparation of a ring ketone of the aromatic series.
PROFELD K dějinám podkrkonošského Inářství a plátenictví.
DE483148C (en) Process for the preparation of oxydiaryl ketones
DE1809962U (en) INSULATING COVER.