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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432081Generated: October 26, 2026

Water → [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanol

https://huagongshe.com/reaction/432081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant(2R)-6-Iodochromane-2-carboxylic acidHCID 9966213—
SolventTetrahydrofuranHCID 8028—
Product[(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanolHCID 9943850—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of (2R)-6-iodo-3,4-dihydro-2H-chromene-2-carboxylic acid (Example 7, 19.5 mmol, 1.0 eq.) in THF (45 mL) at 10° C. was added dropwise a solution of borane-THF complex (1M in THF, 23.4 mmol, 1.2 eq). The resulting reaction mixture was stirred at 45° C. for 1.5 hours and was then cooled to 10° C. Next, water was added followed by saturated NaHCO3 solution. The resulting two-phase mixture was separated and the aqueous phase was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, concentrated to afford the product as a white solid in quantitative yield that was used without further purification. GC-MS m/z 290 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660752B2
Source datasetuspto-grants-2003_12
ORD IDord-9f9d4a6bdbcd444f8483b577369ce20a
Source noteuspto-grants-2003_12