HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 136341174, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 135430562 | HCID 135430562 | — |
| Product | HCID 136341174 | HCID 136341174 | 48% |
Reaction Steps
Following the above procedure for the preparation of 8-(2-propenylmercapto)guanosine (Example 6), but substituting 2-butenyl chloride for allyl bromide, the title compound was obtained in 48 percent yield as a white powder, mp 210° C. (decomp.). NMR (DMSO-d6): δ6.3 (bs, 2H); 5.6 (d, J=5Hz, 1H); 1.6 (d, J=6Hz, 3H). IR (KBr): 1690, 1630, 1600, 1510 and 1365 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05093318 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-f272967320804571a15de6b7edd94907 |
| Source note | uspto-grants-1992_03 |