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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80571Generated: October 27, 2026

Tetrahydrofuran → tert-butyl 4-[(1S)-1-hydroxyethyl]benzoate

https://huagongshe.com/reaction/80571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiethanolamineHCID 8113—
ReactantChlorobis((1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl)boraneHCID 11131038—
Reactanttert-Butyl 4-acetylbenzoateHCID 13844704—
SolventHexaneHCID 8058—
Producttert-butyl 4-[(1S)-1-hydroxyethyl]benzoateHCID 70815081103.3%

Reaction Steps

To tert-butyl 4-acetylbenzoate (3.33 g) in a tetrahydrofuran (23 ml) solution, (−)-B-chlorodiisopinocampheylborane in a 65% hexane solution (11.2 ml) was added dropwise under ice cooling, then the mixture was stirred at that temperature for 1.5 hours. The reaction solution was concentrated, and the residue was diluted by diethyl ether. To the thus solution obtained, diethanolamine (4.3 ml) was added under ice cooling, and the mixture was stirred at room temperature for 2 hours. The precipitates were removed by filtration, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, hexane/ethyl acetate=9/1 to 4/1) to obtain the title compound (3.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846660B2
Source datasetuspto-grants-2014_09
ORD IDord-1a363a750112412691c011c2365672b9
Source noteuspto-grants-2014_09