HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364683Generated: October 31, 2026
HCID 13391105, compound → HCID 13391106, compound
https://huagongshe.com/reaction/364683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 13391105 | HCID 13391105 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13391106 | HCID 13391106 | — |
Reaction Steps
To a stirred solution of 4,5-dihydronaphtho[1,2-b]thiophen-6-carboxylic acid (3.4 g, 0.015 mole) in 50 ml of tetrahydrofuran under an argon atmosphere was added dropwise borane-tetrahydrofuran complex (2.5 g, 0.030 mole). Upon complete addition, the reaction mixture was stirred at room temperature for 18.5 hours. The reaction mixture was then taken up in water and concentrated under reduced pressure to a residue. The residue was washed into a separatory funnel with aqueous 2N sodium hydroxide and methylene chloride. The aqueous layer was extracted with two 100 ml portions of methylene chloride. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give 4,5-dihydronaphtho[1,2-b]thiophen-6-methanol; 2.8 g, mp 99°-100°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04605748 |
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| Source dataset | uspto-grants-1986_08 |
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| ORD ID | ord-c224dd267958407eb68cda74df37aab9 |
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| Source note | uspto-grants-1986_08 |
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