GB276571A - Manufacture of aromatic tetrahydronaphthylamines or derivatives thereof - Google Patents

Manufacture of aromatic tetrahydronaphthylamines or derivatives thereof

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Publication number
GB276571A
GB276571A GB524527A GB524527A GB276571A GB 276571 A GB276571 A GB 276571A GB 524527 A GB524527 A GB 524527A GB 524527 A GB524527 A GB 524527A GB 276571 A GB276571 A GB 276571A
Authority
GB
United Kingdom
Prior art keywords
naphthylamine
ethyl
eliminated
sulphuric acid
acetyl
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
GB524527A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Priority to GB524527A priority Critical patent/GB276571A/en
Publication of GB276571A publication Critical patent/GB276571A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

276,571. Imray, O. Y., (Soc. of Chemical Industry in Basle). Feb. 24, 1927. Ar-Tetrahydronaphthylamine derivatives are obtained by subjecting N-substituted naphthylamines to catalytic hydrogenation; the hydrogenated naphthylamines themselves may be obtained by using an acetyl derivative as the starting material and subsequently saponifying. In examples, (1) ar-N-ethyltetrahydro-a-naphthylamine is obtained bv dissolving N-ethyl-a-naphthylamine in alcohol and treating the solution with hydrogen under pressure in the presence of a nickel catalyst; in the same way ar-N-ethyltetrahydro-#-naphthylamine is obtained from N-.ethyl- #-naphthylamine, and a-acetaminotetrahydronaphthalene from acetyl-a-naphthylamine; the acetyl group may be subsequently eliminated by sulphuric acid: (2) ar-acetyltetrahydro-#-naphthalide is obtained by dissolving acatyl-#-naphthylamine in tetrahydronaphthalene and treating with hydrogen as before; the acetyl group may be eliminated with sulphuric acid. giving tetrahydro-#- naphthylamine ; (3) ar-N-phenyltetrahydro-a-naphthylamine is obtained by hydrogenation of N- phenyl-a-naphthylamine in alcohol and distillation in vacuo in the same way acetylated artetrahydro-N-ethyl-a-naphthylamine is obtained from acetylated N-ethyl-a-naphthylamine; the acetyl group may be eliminated with sulphuric acid.
GB524527A 1927-02-24 1927-02-24 Manufacture of aromatic tetrahydronaphthylamines or derivatives thereof Expired GB276571A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB524527A GB276571A (en) 1927-02-24 1927-02-24 Manufacture of aromatic tetrahydronaphthylamines or derivatives thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB524527A GB276571A (en) 1927-02-24 1927-02-24 Manufacture of aromatic tetrahydronaphthylamines or derivatives thereof

Publications (1)

Publication Number Publication Date
GB276571A true GB276571A (en) 1927-09-01

Family

ID=9792430

Family Applications (1)

Application Number Title Priority Date Filing Date
GB524527A Expired GB276571A (en) 1927-02-24 1927-02-24 Manufacture of aromatic tetrahydronaphthylamines or derivatives thereof

Country Status (1)

Country Link
GB (1) GB276571A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2977308A (en) * 1952-04-23 1961-03-28 Bayer Ag Tetrahydronaphthylamino compounds
US7902191B2 (en) * 2004-02-25 2011-03-08 Eli Lilly And Company Histamine H3 receptor antagonists, preparation and therapeutic uses

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2977308A (en) * 1952-04-23 1961-03-28 Bayer Ag Tetrahydronaphthylamino compounds
US7902191B2 (en) * 2004-02-25 2011-03-08 Eli Lilly And Company Histamine H3 receptor antagonists, preparation and therapeutic uses

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