HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091286Generated: November 2, 2026
Water → 2-[1-(Diphenylmethyl)azetidin-3-yl]ethan-1-ol
https://huagongshe.com/reaction/1091286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Ethyl [1-(diphenylmethyl)azetidin-3-ylidene]acetate | HCID 53428664 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[1-(Diphenylmethyl)azetidin-3-yl]ethan-1-ol | HCID 53440890 | 76% |
Reaction Steps
Lithium aluminumhydride (889 mg, 23.4 mmol) was suspended in tetrahydrofuran (50 mL), and under a nitrogen stream, a tetrahydrofuran (30 mL) solution of (1-benzhydrylazetidin-3-ylidene)acetic acid ethyl ester (2.40 g, 7.81 mmol) was added dropwise over 20 minutes at 0° C. with stirring. The reaction liquor was stirred for two hours at the same temperature, and then while cooling the reaction liquor in ice, water (889 μl), 1 N sodium hydroxide (889 μl) and water (8.57 mL) were added in this order. The resulting mixture was dried over anhydrous sodium sulfate. The insoluble was separated by filtration, and the mother liquor was concentrated under reduced pressure. The obtained residue was purified by flash chromatography (Flash Chromatography System from Biotage AB, column size: 40M, ethyl acetate:n-hexane=1:1 to ethyl acetate), to obtain the title compound (1.58 g, 76%) as an oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129366B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-8a366174f1ef4939bfdc9cf244f2fffa |
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| Source note | uspto-grants-2012_03 |
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