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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294047Generated: October 30, 2026

Tetrahydrofuran → Tert-butyl 6-triphenylmethyloxy-3(R),5(S)-dihydroxyhexanoate

https://huagongshe.com/reaction/1294047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiethylmethoxyboraneHCID 522516—
ReactantSodium borohydrideHCID 4311764—
Reactantt-Butyl (S)-5-hydroxy-3-oxo-6-(triphenylmethoxy)hexanoateHCID 15702750—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductTert-butyl 6-triphenylmethyloxy-3(R),5(S)-dihydroxyhexanoateHCID 57144739—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To the crude tert-butyl 6-triphenylmethyloxy-5(S)-hydroxy-3-oxohexanoate was added 150 mL of THF followed by 15 mL of MeOH and was chilled to −60° C. 26 mL of methoxydiethylborane (50% solution in THF) was added over a period of 20 minutes and stirring was continued for a further 30 minutes. The reaction mixture was cooled to −80° C. and 5 g of sodium borohydride was added in portions and the after completion of addition the reaction mixture was stirred for 5 hours at −78° C. Acetic acid was added to adjust the pH to 7 and water was added. The aqueous layer was extracted using EtOAC, washed with brine, dried and concentrated to give the title compound which was used as such for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238826B2
Source datasetuspto-grants-2007_07
ORD IDord-d837fa3e0b3a4cbd9584ec037cfbf126
Source noteuspto-grants-2007_07