HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852293Generated: October 30, 2026
Hydrogen Bromide → HCID 20160186, compound
https://huagongshe.com/reaction/852293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Product | HCID 20160186 | HCID 20160186 | 1.4% |
Reaction Steps
Adapting a procedure of Büchi and Wüest (J. Org. Chem, 1969, 34, 1122–1123), crotonaldehyde (3 g, 43 mmol) was added dropwise to cone. aq. HBr (5.2 g, 64 mmol) over 5 min at 5° C. under air atmosphere. After 15 min of stirring at 5° C. during which time the mixture changed from colourless to brownish, 1,3-propanediol (8.1 g, 107 mmol) was added and the reaction was stirred at 5° C. for further 0.5 h before allowing it warn to rt, and finally stirring it at rt for 2 h. The crude reaction mixture was then n-heptane extracted (2×200 mL), the combined n-heptane extracts were Na2SO4 dried, evaporated in vacuo and 121JP80 was isolated by Kugelrohr distillation (75° C., 0.18 mmHg) to obtain 124 mg (1.4%) of the title compound as a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253186B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-b2952cce38864106b2d7b07053c495e7 |
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| Source note | uspto-grants-2007_08 |
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