HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263322Generated: October 30, 2026
5,6,7,8-Tetrahydronaphthalene-1,6-diol → 1,2,3,4-Tetrahydro-5-[2,3-epoxy-propoxy]-2-naphthol
https://huagongshe.com/reaction/263322
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5,6,7,8-Tetrahydronaphthalene-1,6-diol | HCID 12445738 | — |
| Reactant | Naphthalen-1(2H)-one | HCID 12446728 | — |
| Product | 1,2,3,4-Tetrahydro-5-[2,3-epoxy-propoxy]-2-naphthol | HCID 12445767 | — |
Reaction Steps
Employing the procedure of Example 3a, but substituting a 6-alkoxy-1-tetralone as shown in the left hand (first) column of Table II for 6-methoxy-1-tetralone, a 6-alkoxy-1-naphthol is produced, which is converted as per Example 3b to the corresponding 5-hydroxy-3,4-dihydro-2(1H)-naphthalenenone shown in the middle column of Table II; employing the procedure of Example 3c the naphthalenone is converted to the corresponding 5,6,7,8-tetrahydro-1,6-naphthalenediol which is reacted with an epoxide of the structure ##STR52## in accordance with the procedure of Example 3d to form the corresponding 1,2,3,4-tetrahydro-5-[2,3-epoxy-propoxy]-2-naphthol which is reacted with an amine of the structure ##STR53## in accordance with the procedure of Example 3e to form the corresponding 1,2,3,4-tetrahydro-5-[2-hydroxy-3-(R1, R2 -substituted amino)propoxy]-2-naphthol (formula I) as shown in the right hand (third) column of Table II.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04156789 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-1312e13fe4f748ff8ac8b0d0e1bbd214 |
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| Source note | uspto-grants-1979_05 |
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