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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762137Generated: November 2, 2026

Water → HCID 131715947, compound

https://huagongshe.com/reaction/1762137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactanttrans-2,2-Dimethyl-3-bromo-6-cyanochroman-4-olHCID 6932483—
Reactant3-[(Trimethylsilyl)oxy]pyrrolidin-2-oneHCID 13385941—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 131715947HCID 131715947—

Reaction Steps

Sodium hydride (80% dispersion in oil, 1.6 g) was added to a solution of (±)-6-cyano-3,4-dihydro-2,2-dimethyl-trans-3-bromo-4-hydroxy-2H-1-benzopyran (14.86 g) in DMSO (100 mL) and the mixture stirred under a dry atmosphere for 45 min when a solution of the 3,4-epoxide resulted. The solution was then cooled to ca 10° C. before 3-trimethylsilyloxy-2-pyrrolidinone (12.86 g) was added along with further DMSO (20 mL) and sodium hydride (2.35 g). The mixture was stirred at room temperature for 22 h after which it was poured into water (600 mL) and extracted with ethyl acetate several times. The combined extracts were washed with water (4×150 mL), brine and dried (Na2SO4). Evaporation gave a crystalline greenish solid (14.4 g) which was triturated with a little ethyl acetate before filtering under suction and washing with a little ethyl acetate followed by 50% ether/ethyl acetate. The crystalline material (7.9 g, 50%) appeared to be a ca 50:50 mixture of the 3'-hydroxy isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831050
Source datasetuspto-grants-1989_05
ORD IDord-adfea2f81bba4277be10532e21a0908a
Source noteuspto-grants-1989_05