HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropanecarboxaldehyde → HCID 90253544, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Reactant | HCID 12285346 | HCID 12285346 | — |
| Reactant | HCID 42604962 | HCID 42604962 | — |
| Product | HCID 90253544 | HCID 90253544 | — |
Reaction Steps
Using the method described by J. Nokami et al., J. Am. Chem. Soc. 2001, 123, 9168-9169, cyclopropanecarbaldehyde was reacted with (1S,2R,5S)-1-[(2S)-but-3-en-2-yl]-5-methyl-2-(propan-2-yl)cyclohexanol [this crotylation reagent was derived from (+)-menthol] to afford the product as an oil. Yield: 600 mg, 4.75 mmol, 100%. 1H NMR (400 MHz, CDCl3), characteristic peaks: δ 5.45-5.63 (m, 2H), 2.86-2.92 (m, 1H), 2.33-2.41 (m, 1H), 2.20-2.29 (m, 1H), 1.69-1.72 (m, 3H), 0.47-0.56 (m, 2H), 0.27-0.37 (m, 1H), 0.16-0.26 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403846B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-23df10c1cd564176a3ed03cfaed6b0ec |
| Source note | uspto-grants-2016_08 |