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公开(公告)号:CA790617A
公开(公告)日:1968-07-23
申请号:CA790617D
Applicant: ALLIED CHEM
Inventor: HOLLANDER JEROME , WOOLF CYRIL
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公开(公告)号:CA777814A
公开(公告)日:1968-02-06
申请号:CA777814D
Applicant: ALLIED CHEM
Inventor: WOOLF CYRIL , HOLLANDER JEROME
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公开(公告)号:DE1246706B
公开(公告)日:1967-08-10
申请号:DEA0044106
申请日:1963-09-20
Applicant: ALLIED CHEM
Inventor: ANELLO LOUIS GENE , NYCHKA HENRY ROBERT , WOOLF CYRIL
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公开(公告)号:CA746951A
公开(公告)日:1966-11-22
申请号:CA746951D
Applicant: ALLIED CHEM
Inventor: SILVERSTEIN ROBERT M , MILL THEODORE , RODIN JOHN O , WOOLF CYRIL
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公开(公告)号:DE1216277B
公开(公告)日:1966-05-12
申请号:DEA0043214
申请日:1963-05-29
Applicant: ALLIED CHEM
Inventor: ANELLO LOUIS GENE , WOOLF CYRIL
IPC: C07C17/10
Abstract: 2,2-Chlorofluoropropane is prepared by subjecting a gaseous mixture of one mole of isopropyl fluoride and at least one mole of chlorine in a reaction zone to actinic radiation for 0.5-200 seconds while maintaining the temperature in said zone below 150 DEG C. but high enough to retain the reactants in the gaseous phase. The actinic radiation is preferably of wavelength 2,000-5,000 Angstrom units and is preferably supplied by an artificial light source. 3-Chloro-2-fluoropropane and 2,3-dichloro-2-fluoropropane are obtained as by-products. Examples are given.
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公开(公告)号:DE1210772B
公开(公告)日:1966-02-17
申请号:DEA0043475
申请日:1963-07-01
Applicant: ALLIED CHEM
Inventor: HOLLANDER JEROME , WOOLF CYRIL
IPC: B01J23/86 , C07C29/145
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公开(公告)号:DE1199754B
公开(公告)日:1965-09-02
申请号:DEA0044107
申请日:1963-09-20
Applicant: ALLIED CHEM
Inventor: NYCHKA HENRY ROBERT , WOOLF CYRIL
IPC: B01J23/26 , C07C45/63 , C07C49/16 , C07C49/167
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公开(公告)号:CA706922A
公开(公告)日:1965-03-30
申请号:CA706922D
Applicant: ALLIED CHEM
Inventor: ANELLO LOUIS G , NYCHKA HENRY R , WOOLF CYRIL
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公开(公告)号:DE1176118B
公开(公告)日:1964-08-20
申请号:DEA0041308
申请日:1962-10-03
Applicant: ALLIED CHEM
Inventor: GORDON JOSEPH , WOOLF CYRIL
IPC: C07C31/34
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公开(公告)号:DE1173440B
公开(公告)日:1964-07-09
申请号:DEA0042804
申请日:1961-12-14
Applicant: ALLIED CHEM
Inventor: ANELLO LOUIS GENE , WOOLF CYRIL
IPC: C01B21/084
Abstract: Nitrosyl fluoride complexes NOF.3HF boiling at 95 DEG C. and NOF.6HF boiling at 68 DEG C. at atmospheric pressure are prepared by reacting together nitrosyl chloride and hydrogen fluoride under anhydrous conditions. The reaction may be batchwise or continuous, in the gas or liquid phases, at reduced or superatmospheric pressures between - 25 DEG C. and 250 DEG C. The NOC1 may be replaced by a mixture of chlorine and nitric oxide with an activated carbon catalyst. The mol. ratio of HF : NOC1 is between 3 : 1 and 8 : 1. The complexes may be dehydrofluorinated by alkali metal fluoride, e.g. NaFn HF or KFn HF where the mol. ratio of KF to HF is preferably between 1 : 2 and 1 : 4 with the complex in the liquid phase below 95 DEG C. or in the gas phase in the range 100-150 DEG C. in a batchwise or continuous process.
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