HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825791Generated: November 1, 2026
Borane;tetrahydrofuran → HCID 22139447, compound
https://huagongshe.com/reaction/1825791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 22139400 | HCID 22139400 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22139447 | HCID 22139447 | 99.8% |
Reaction Steps
To a cooled (0° C.) suspension of 4-benzyloxy-1-(4-methoxy-benzylamino)-thioxanthen-9-one (8.16 g, 18.00 mmol) in dry THF (150 ml) was added Borane-THF complex (90 mmol, 90 ml 1M in THF) in a dropwise fashion. The reaction was allowed to slowly warm to room temperature and stirred for a further 16 hours to give a homogeneous yellow solution. To mixture was then cooled (0° C.) and diluted slowly with acetone (150 ml) and then stirred for 60 minutes at room temperature. The solvent was removed in vacuo to give a crude residue that was diluted in CH2Cl2 (100 ml) and the washed with a saturated solution of NaHCO3 (100 ml), dried using MgSO4, filtered and concentrated in vacuo to give the title compound as a mild amber oil (7.90 g, 99.8%) m/z (LC-MS, ESP): 438 [M+H]+, R/T=5.01 mins.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07049313B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-ee6e947d05084e5a99733332068947e4 |
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| Source note | uspto-grants-2006_05 |
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