HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioxanthone → 9H-thioxanthen-9-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioxanthone | HCID 10295 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 9H-thioxanthen-9-ol | HCID 5154170 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806283B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-5a0f4c1e54344c8ca6ce20442184321b |
| Source note | uspto-grants-2004_10 |