BE358148A - - Google Patents

Info

Publication number

BE358148A

BE358148A BE358148DA BE358148A BE 358148 A BE358148 A BE 358148A BE 358148D A BE358148D A BE 358148DA BE 358148 A BE358148 A BE 358148A

Authority

BE

Belgium

Prior art keywords

pinene

acid

ether

ethers

acids

Prior art date

Links

• Espacenet
• Global Dossier
• Discuss

• JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 8
• 239000003054 catalyst Substances 0.000 claims description 4
• 150000002170 ethers Chemical class 0.000 claims description 4
• 239000000203 mixture Substances 0.000 claims description 4
• 238000006266 etherification reaction Methods 0.000 claims description 3
• 238000000034 method Methods 0.000 claims description 3
• 150000007524 organic acids Chemical class 0.000 claims description 3
• DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 2
• KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
• 239000004327 boric acid Substances 0.000 claims description 2
• 239000003921 oil Substances 0.000 claims description 2
• 235000005985 organic acids Nutrition 0.000 claims description 2
• 150000007522 mineralic acids Chemical class 0.000 claims 1
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 17
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
• MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
• -1 bornyl ether Chemical compound 0.000 description 4
• 239000002253 acid Substances 0.000 description 3
• 150000007513 acids Chemical class 0.000 description 3
• 150000008064 anhydrides Chemical class 0.000 description 3
• 239000000706 filtrate Substances 0.000 description 3
• 235000011007 phosphoric acid Nutrition 0.000 description 3
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
• 230000002378 acidificating effect Effects 0.000 description 2
• 230000015572 biosynthetic process Effects 0.000 description 2
• 238000001914 filtration Methods 0.000 description 2
• 238000010992 reflux Methods 0.000 description 2
• DTGKSKDOIYIVQL-UHFFFAOYSA-N Borneol Chemical compound C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
• GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
• 241000779819 Syncarpia glomulifera Species 0.000 description 1
• 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
• 239000006227 byproduct Substances 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• 230000000295 complement effect Effects 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 238000004821 distillation Methods 0.000 description 1
• 238000002844 melting Methods 0.000 description 1
• 230000008018 melting Effects 0.000 description 1
• 229910017604 nitric acid Inorganic materials 0.000 description 1
• 239000001739 pinus spp. Substances 0.000 description 1
• 239000011269 tar Substances 0.000 description 1
• LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical group CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
• 229940036248 turpentine Drugs 0.000 description 1
• 238000005292 vacuum distillation Methods 0.000 description 1
• 239000002023 wood Substances 0.000 description 1