HuagongsheHuagongshe Chemistry Print Report · For research reference only
[(R)-2-(2,2-diethoxyethoxy)-4-pentenyloxymethyl]benzene → HCID 90253549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [(R)-2-(2,2-diethoxyethoxy)-4-pentenyloxymethyl]benzene | HCID 59281174 | — |
| Reactant | HCID 90253544 | HCID 90253544 | — |
| Product | HCID 90253549 | HCID 90253549 | — |
Reaction Steps
(1R,3E)-1-Cyclopropylpent-3-en-1-ol (C24) was converted to the product according to the method used for the synthesis of ({[(2R)-2-(2,2-diethoxyethoxyl)pent-4-en-1-yl]oxy}methyl)benzene (C2) in Preparation P1, except that all reagents were combined at 0° C. The product was obtained as a colorless oil. Yield: 550 mg, 2.27 mmol, 48%. 1H NMR (400 MHz, CDCl3) δ 5.44-5.59 (m, 2H), 4.62 (dd, J=5.3, 5.3 Hz, 1H), 3.66-3.76 (m, 3H), 3.54-3.63 (m, 2H), 3.47 (dd, J=10.3, 5.5 Hz, 1H), 2.65 (dt, J=8.5, 5.9 Hz, 1H), 2.28-2.33 (m, 2H), 1.65-1.68 (m, 3H), 1.23 (t, J=7.1 Hz, 3H), 1.23 (t, J=7.0 Hz, 3H), 0.79-0.88 (m, 1H), 0.53-0.60 (m, 1H), 0.42-0.50 (m, 1H), 0.34-0.41 (m, 1H), 0.06-0.13 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403846B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-093f2a2b0a2a40879797508b11948475 |
| Source note | uspto-grants-2016_08 |