HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479387Generated: October 31, 2026
Sodium borohydride → HCID 69492381, compound
https://huagongshe.com/reaction/479387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 18770408 | HCID 18770408 | — |
| Solvent | 2-(Oxolan-2-yl)ethan-1-ol | HCID 11989572 | — |
| Product | HCID 69492381 | HCID 69492381 | 97.3% |
Reaction Steps
Under ice cooling, calcium chloride (968 mg; 8.8 mmol) and sodium borohydride (668 mg; 17 mmol) were added to a solution in tetrahydrofuran-ethanol (9 ml-14 ml) of methyl 2,2-bis[(1-tert-butoxycarbonyl-4-piperidinyl)-methyl]acetate (1.0 g; 2.1 mmol) synthesized by the process described in Referential Example 3, and the mixture was stirred for 2 hours. The reaction mixture was concentrated under reduced pressure, and the resultant concentrated residue was dissolved in chloroform. The solution was washed successively with 3N hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 900 mg (yield: 96%) of 2,2-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]ethyl alcohol as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645957B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-fce09ebbcdab475eb8ac8dd4f2e17346 |
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| Source note | uspto-grants-2003_11 |
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