HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 23324610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 178440239 | HCID 178440239 | — |
| Product | HCID 23324610 | HCID 23324610 | — |
Reaction Steps
4-Chloromethyl-6-hydroxy-2-isopropyl-pyrimidine is reacted with allylbromide analogously to the process described in Example 86 in order to produce 4-chloromethyl-2-isopropyl-6-(2-propenyloxy)-pyrimidine which is required as the starting material in Example 24. This product is obtained in the form of an oil, 1H-NMR (CDCl3): 1.30 (d, 2×CH3), 3.15 (m, CH), 4.55 (s, CH2), 4.93 (m, CH2), 5.37 (m, CH2), 6.12 (m, CH), 6.75 (s, CH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04584295 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-4b75a929d50f4e09a3316f5ec590a577 |
| Source note | uspto-grants-1986_04 |