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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594450Generated: October 30, 2026

Acetic Acid → Tert-butyl 6-triphenylmethyloxy-3,5-dihydroxyhexanoate

https://huagongshe.com/reaction/1594450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl 6-triphenylmethyloxy-5-hydroxy-3-oxohexanoateHCID 19778647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 6-triphenylmethyloxy-3,5-dihydroxyhexanoateHCID 11374654—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To the crude tert-butyl 6-triphenylmethyloxy-5-hydroxy-3-oxohexanoate was added 150 mL of THF followed by 15 mL of MeOH and was chilled to −60° C. 26 mL of MDEB (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 numberUS07301046B2
Source datasetuspto-grants-2007_11
ORD IDord-9ab2539a0287423d8375aed3b4dd3da7
Source noteuspto-grants-2007_11