HuagongsheHuagongshe Chemistry Print Report · For research reference only
Crotonaldehyde → HCID 536251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Product | HCID 536251 | HCID 536251 | — |
Reaction Steps
Thioacetic acid (385 mL, 5.4 mol, commercially available from Sigma-Aldrich, Inc., Inc.) and crotonaldehyde (440 mL, 5.4 mol, commercially available from Acros Organics) were used to provide 3-(acetylthio)butanal (640 g), which was treated with sodium borohydride (NaBH4, commercially available from Acros Organics) to provide 3-acetylthio-1-butanol, which was consequently hydrolyzed, and distilled under vacuum to provide the product of 3-mercapto-1-butanol (165 g), which had boiling points of 90° C. at a pressure of 29 mmHg, and 85° C. at 18 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598110B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-562877e42e814ef8906f24df9093eea8 |
| Source note | uspto-grants-2013_12 |