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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056759Generated: November 2, 2026

Sodium borohydride → [(1S)-1-(2-{[tert-Butyl(diphenyl)silyl]oxy}ethyl)-3,4-dihydro-1H-2-benzopyran-6-yl]methanol

https://huagongshe.com/reaction/2056759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(1S)-1-(2-{[tert-Butyl(diphenyl)silyl]oxy}ethyl)-3,4-dihydro-1H-2-benzopyran-6-carbaldehydeHCID 86596016—
SolventEthanolHCID 702—
Product[(1S)-1-(2-{[tert-Butyl(diphenyl)silyl]oxy}ethyl)-3,4-dihydro-1H-2-benzopyran-6-yl]methanolHCID 69310633—

Reaction Steps

To a stirred solution of (1S)-1-(2-{[tert-butyl(diphenyl)silyl]oxy}ethyl)-3,4-dihydro-1H-2-benzopyran-6-carbaldehyde (0.97 g, 2.18 mmol) in ethanol (30 mL) was added sodium borohydride (0.116 g, 3.06 mmol) and the mixture stirred for 1.5 h at room temperature. The reaction was extracted from water into ethyl acetate, the combined organic extracts dried (MgSO4), filtered and evaporated in vacuo, to yield the title compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335660B2
Source datasetuspto-grants-2008_02
ORD IDord-91f0d5efc46d4c9f8809017e142bf78f
Source noteuspto-grants-2008_02