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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393259Generated: October 26, 2026

Thioxanthone → 9H-thioxanthen-9-ol

https://huagongshe.com/reaction/393259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioxanthoneHCID 10295—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product9H-thioxanthen-9-olHCID 515417093%

Reaction Steps

A suspension of thioxanthen-9-one [31] (2 g, 9.42 mmol) in anhydrous CH3OH (30 mL) was stirred under N2 and NaBH4 (1.42 g, 37.68 mmol) was added slowly in portions over 15 min. After complete addition the reaction mixture was heated at reflux (3 hr.) and cooled to room temperature. Ice-water was added and the reaction mixture was extracted with CH2Cl2 (3×50 mL). The combined CH2Cl2 extracts were washed with water, brine, dried (MgSO4). The solvent was removed under reduced pressure to give a yellow solid, which was recrystallized from pet.ether to give 1.87 g (93%) of the alcohol as pale yellow needles, mp 104-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806283B2
Source datasetuspto-grants-2004_10
ORD IDord-5a0f4c1e54344c8ca6ce20442184321b
Source noteuspto-grants-2004_10