DE90908C - - Google Patents

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Publication number

DE90908C

DE90908C DENDAT90908D DE90908DA DE90908C DE 90908 C DE90908 C DE 90908C DE NDAT90908 D DENDAT90908 D DE NDAT90908D DE 90908D A DE90908D A DE 90908DA DE 90908 C DE90908 C DE 90908C

Authority

DE

Germany

Prior art keywords

formaldehyde

mol

instead

hydroxyl groups

substituted

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.)

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• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 23
• -1 aromatic hydroxy compounds Chemical class 0.000 claims description 7
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
• 238000000034 method Methods 0.000 claims description 5
• 125000003118 aryl group Chemical group 0.000 claims description 3
• 150000001875 compounds Chemical group 0.000 claims description 3
• 150000001298 alcohols Chemical class 0.000 claims description 2
• WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 2
• 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims 2
• JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 8
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
• ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
• 238000006243 chemical reaction Methods 0.000 description 4
• 150000002989 phenols Chemical class 0.000 description 4
• 150000003335 secondary amines Chemical class 0.000 description 4
• NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
• 238000002844 melting Methods 0.000 description 2
• 230000008018 melting Effects 0.000 description 2
• 150000004780 naphthols Chemical class 0.000 description 2
• 150000003512 tertiary amines Chemical class 0.000 description 2
• MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
• QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
• 239000005844 Thymol Substances 0.000 description 1
• 150000007514 bases Chemical class 0.000 description 1
• 244000309464 bull Species 0.000 description 1
• 229930003836 cresol Natural products 0.000 description 1
• 230000008030 elimination Effects 0.000 description 1
• 238000003379 elimination reaction Methods 0.000 description 1
• 239000000446 fuel Substances 0.000 description 1
• RJUAEBLXGFKZMS-UHFFFAOYSA-N piperidin-1-ylmethanol Chemical class OCN1CCCCC1 RJUAEBLXGFKZMS-UHFFFAOYSA-N 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 229960000790 thymol Drugs 0.000 description 1