HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 11760840, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 131719198 | HCID 131719198 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Toluene ethylacetate | HCID 21584019 | — |
| Product | HCID 11760840 | HCID 11760840 | — |
Reaction Steps
To a mixture of β-lactose peracetate (50 g), ethanethiol (6.9 g, 822 ml) and 200 ml dry CH2Cl2 was added BF3 /Et2O (8.5 g, 7.3 ml) at RT. After 2 hours, TLC (toluene/ethyl acetate 2/3) showed no more reaction. The mixture was shaken with ca 500 ml 1M NaOH. The organic layer was directly evaporated and taken up in methanol (150 ml), then NaOMe in methanol (10 ml, 0.5M) was added and the mixture was stirred overnight at RT. The TLC (ethyl acetate/acetic acid/methanol/water 12/3/3/3) yields an Rf 0.41. The reaction mixture was neutralized with Dowex (50w×8, H+) filtered and concentrated The residue was recrystallized from ethanol (300 ml). Yield 16.4 g, 56%, mp 191°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466681 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-c86389b304604f4a81ff78a303600601 |
| Source note | uspto-grants-1995_11 |