SCIENTIFIC ABSTRACT GOLDFARB, YA. - GOLDFELD, I.
Document Type:
Collection:
Document Number (FOIA) /ESDN (CREST):
CIA-RDP86-00513R000515620020-0
Release Decision:
RIF
Original Classification:
S
Document Page Count:
100
Document Creation Date:
November 2, 2016
Document Release Date:
September 26, 2002
Sequence Number:
20
Case Number:
Publication Date:
December 31, 1967
Content Type:
SCIENTIFIC ABSTRACT
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JI 0 "J
Reducing Degulfurization of' Some Diamines of' the S/WO/60 /1 1/05/037/C) I'
Thiophene Series B011/BJ17
less active than skeleton nickel. ilctually, the amines III and II1a slowly lose
their sulfur, when heated in methanol with a larCe excess o~ cobalt. The dia-Minez-
IV and IVa can be obtained in the ordinary way when desulfuriza-tior. is finished.
The yields were not in excess of 30,'Z'), it is true, but the authors 'have ood
reason to presume that this yield was poss,.bly due to some changeB of the
experimental conditions. From the amines mentioned, diiodo inethyl&tes IV and
IVa were prepared, The investigation is continued. There are 3 references, 31 of
which are Soviet.
ASSOCIATION: institut orcanicheskoy khimii im- N~ D,. Zelin3koGo Akaderr.4i nauk
SSSR (Institute of Oreanic Chemistry imeni N. D, Zelinski~ of. the
Academy of Sciences, US R).Mo3kovsl-,iy fiziko-tekanicheskiy institut
Ch-loscow Institute of Phy3ics and Engineering)
PRESENTED. December 16, 1959~ by A. A. Balandin, Academici-~--.n
SUBMITTED: December 6, 1959
Card 212
GOLIDFAITIB, Ya.L.; KONDAHOVA, M.S.
Synthesis of bifunctiqnfd derivatives from 2, 5 .. d:Lnie thyl. thi ophene.
Report No.2: Action of amines on 3, 4-bls(chlorouiethyl)-2, 5--
dimethylthiophene. Izv.All SSSR Otd.khi-m.nauk n0.3.501-513 Mr 161.
(,ERA 14:4)
1. Institut organicheskoy khimii imeni N.D.Zeliwkogo All 336.q.
0
(Thiophone) (Amince)
GOLIDFALb, Ya.L.; j1d;TIK, L.V,; Fb,TUKliOV, V.A.
Nitration products of o