HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723457Generated: October 25, 2026
Tetrahydrofuran → tert-Butyl 4-azido-3-hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/723457
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | (+/-)-Tert-butyl 4-azido-3-oxopiperidine-1-carboxylate | HCID 21874153 | — |
| Solvent | Water | HCID 962 | — |
| Product | tert-Butyl 4-azido-3-hydroxypiperidine-1-carboxylate | HCID 21874176 | — |
Reaction Steps
To a solution of Compound 201A prepared above in dry THF (2 mL) cooled at −78° C. was added L-Selectride (1.0 M in THF, 0.98 mL, 0.98 mmol). The mixture was stirred at −78° C. for 2.0 hrs. Saturated NH4Cl (2 mL) was added and the reaction mixture was allowed to warm to room temperature. The mixture was diluted with water and extracted with EtOAc (3×). The combined organic layers were washed once with brine and dried over anhydrous Na2SO4. Concentration in vacuo followed by flash chromatography (hexane-EtOAc 4:1) on silica gel gave 44 mg of Compound 201B as an oil. 1H-NMR (400 MHz, CDCl3): 3.84 (m, 1H), 3.69 (m, 1H), 3.58 (m, 2H), 3.40 (m, 1H), 3.30 (m, 1H), 1.96 (m, 1H), 1.73 (m, 1H), 1.46 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141571B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-d058b9f470174969b4623e7ee84d6d73 |
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| Source note | uspto-grants-2006_11 |
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