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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736492Generated: October 30, 2026

Sodium borohydride → HCID 9818164, compound

https://huagongshe.com/reaction/1736492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19433114HCID 19433114—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventEthanolHCID 702—
ProductHCID 9818164HCID 981816461.3%

Reaction Steps

A stirred solution of 3-(3-cyclopentyloxy-4-methoxyphenyl)-4,5-dihydrothiophene 1,1-dioxide (1.2 g; which is prepared as described in Example 13) in ethanol (50 mL) is treated with sodium borohydride (0.45 g) followed by cobalt dichloride hexahydrate (0.94 g), and the purple mixture is stirred at room temperature for 6 hours. It is then filtered through a pad of diatomaceous earth, and the pad is washed with dichloromethane (150 mL). The combined flitrate and washings are evaporated, and the resulting residue is subjected to flash chromatography on silica gel, using a mixture of ethyl acetate and toluene as eluent, to give an oil which slowly crystallizes. It is recrystallized from ethyl acetate at -40° C., to give 3-(3-cyclopentyloxy-4methoxyphenyl)tetrahydrothiophene 1,1-dioxide (0.74 g) in the form of a white solid, m.p. 89°-90° C. [Elemental analysis: C,61.8; H,7.10; S,10.4%; calculated: C,61.91; H,7.1; S,10.33%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541219
Source datasetuspto-grants-1996_07
ORD IDord-b835b252543d4cc798e8e1dc617afc10
Source noteuspto-grants-1996_07