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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922060Generated: October 31, 2026

Crotonaldehyde → HCID 536251, compound

https://huagongshe.com/reaction/1922060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCrotonaldehydeHCID 447466—
ReactantHCID 178418634HCID 178418634—
ProductHCID 536251HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173822B2
Source datasetuspto-grants-2012_05
ORD IDord-fb8f1446d06e4d42961e6e71ab179359
Source noteuspto-grants-2012_05