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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254Generated: October 29, 2026

Tetrahydrofuran → tert-butyl (3R)-4-hydroxy-3-methylbutyrate

https://huagongshe.com/reaction/2254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-tert-butyl (3R)-3-methylsuccinateHCID 86309364—
SolventMethanolHCID 887—
Producttert-butyl (3R)-4-hydroxy-3-methylbutyrateHCID 1072591391.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Borane-dimethyl sulphide complex (10M, 10.3 ml) was added during 15 minutes to a stirred mixture of 1-tert-butyl (3R)-3-methylsuccinate (12.9 g) and THF (200 ml) which had been cooled to -10° C. and placed under an atmosphere of argon. The mixture was stirred at -10° C. for 30 minutes. The mixture was allowed to warm to room temperature and was stirred for 1 hour. The mixture was recooled to 5° C. and methanol (50 ml) was added portionwise. The mixture was allowed to warm to room temperature and was stirred for 30 minutes. The mixture was evaporated and the residue was partitioned between dichloromethane (100 ml) and water (100 ml). The organic phase was filtered through phase separating paper and evaporated to give tert-butyl (3R)-4-hydroxy-3-methylbutyrate as an oil (11 g); NMR(CDCl3) δ 3.55(2H,m), 2.1-2.4(3H,m), 1.46(9H,s), 0.98(3H,d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728701
Source datasetuspto-grants-1998_03
ORD IDord-f546ef0358d64d9eb7bc59ad9f9555cd
Source noteuspto-grants-1998_03