HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713878Generated: October 30, 2026
Tetrahydrofuran → (6-(Spiro[5.5]undecan-3-yloxy)naphthalen-2-yl)methanol
https://huagongshe.com/reaction/713878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | Methyl 6-(spiro[5.5]undecan-3-yloxy)-2-naphthoate | HCID 66926514 | — |
| Product | (6-(Spiro[5.5]undecan-3-yloxy)naphthalen-2-yl)methanol | HCID 66926446 | — |
Reaction Steps
To a solution of 6-(Spiro[5.5]undec-3-yloxy)-naphthalene-2-carboxylic acid methyl ester (0.374 g, 0.00106 mol) in tetrahydrofuran (10 mL, 0.1 mol) was added 1.0 M of lithium tetrahydroaluminate in tetrahydrofuran (3.18 mL, 0.00318 mol) at 0° C. The reaction was then allowed to warm to room temperature while stirring for 2 h, Rochele's salt was then added and stirred the resulting mixture was stirred at room temperature for 1 h. After extraction with ethyl acetate, and solvent removal under vacuum, (6-(spiro[5.5]undecan-3-yloxy)naphthalen-2-yl)methanol was obtained as a while solid (0.28 g, 83%). ESI-MS: 307.5 (M+H)+. 100%). 1H NMR (400 MHz, CDCl3) δ 7.74-7.70 (m, 3H), 7.44 (d, J=10.0 Hz, 1H), 7.16 (m, 2H), 4.81 (s, 2H), 4.40 (m, 1H), 1.94-1.26 (m, 18H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09186367B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-420483a0a2de44bcbad90239a2fdced0 |
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| Source note | uspto-grants-2015_11 |
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