HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074574Generated: October 31, 2026
HCID 13066908, compound → HCID 13066910, compound
https://huagongshe.com/reaction/1074574
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13066908 | HCID 13066908 | — |
| Reactant | HCID 13066909 | HCID 13066909 | — |
| Product | HCID 13066910 | HCID 13066910 | 73.5% |
Reaction Steps
By condensing 1,4-dimethoxy-2-methyl-3-(4-iodobutyl)naphthalene (3.84 g, 10 mmole) with 1-(2-tetrahydropyranyloxy)-2,7-octadiyne (2.10 g, 10 mmole) in accordance with the procedure of the above Reference Example 46, there was produced 1,4-dimethoxy-2-methyl-3-(12-hydroxy-5,10-dodecadiynyl)naphthalene (2.78 g, 73.5%, oily product). 1,4-Dimethoxy-2-methyl-3-(4-iodobutyl)naphthalene [δ1.5 to 2.2(4H), 2.40(3H), 2.82(2H), 3.23(2H), 3.84(3H), 3.87 (3H), 7.3 to 7.5(2H), 7.8 to 8.1(2H)] as utilized in this Reference Example was produced from 1,4-dimethoxy-2-methyl-3-(4-hydroxybutyl)naphthalene [oily substance, NMR (CDCl3), δ1.5 to 1.8(5H), 2.39(3H), 2.81(2H), 3.67(2H), 3.84(3H), 3.87(3H), 7.3 to 7.5(2H), 7.9 to 8.1(2H)] in accordance with the procedure described in Japanese Patent Application No. 49433/'80.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04393075 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-1f10ddd1d0e3467988f2007f30ded727 |
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| Source note | uspto-grants-1983_07 |
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