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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279431Generated: October 31, 2026

Sodium borohydride → HCID 69492381, compound

https://huagongshe.com/reaction/1279431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantCalcium ChlorideHCID 5284359—
ReactantHCID 18770408HCID 18770408—
Solvent2-(Oxolan-2-yl)ethan-1-olHCID 11989572—
ProductHCID 69492381HCID 6949238197.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448242B1
Source datasetuspto-grants-2002_09
ORD IDord-4c45b84c5c8d43a8a653084447a37c04
Source noteuspto-grants-2002_09