Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586905Generated: November 1, 2026

Lithium borohydride → 5-Benzyloxy-1,3-pentanediol

https://huagongshe.com/reaction/1586905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 10879179HCID 10879179—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Benzyloxy-1,3-pentanediolHCID 19760155—

Reaction Steps

To a solution of methyl 3-(S)-hydroxy-5-benzyloxypentanoate (38, Kitamura, M.; Ohkuma, T.; Inoue, S.; Sayo, N.; Kumobayashi, H.; Akutagawa, S.; Ohta, T.; Takaya, H.; Noyori, R., J. Am. Chem. Soc. 1988, 110 629-631) (183 mmol) in anhydrous THF (1 l) is added lithium borohydride (7.7 g, excess) at 0° C. over 15 min. The reaction mixture is stirred at RT for 30 minutes, and then refluxed for 6 hours. The mixture is then cooled to 0° C., diluted with water (60 ml), and stirred overnight at RT. A white precipitate is removed by filtration, the solvent removed in vacuum, and the residue distilled under vacuum to yield 5-benzyloxy-1,3-pentanediol 39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216141
Source datasetuspto-grants-1993_06
ORD IDord-31109c18c3bb4b3283a7183826bd7b1b
Source noteuspto-grants-1993_06