HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → HCID 57608491, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | m-Bromobenzenethiol | HCID 80597 | — |
| Product | HCID 57608491 | HCID 57608491 | — |
Reaction Steps
Alkylation of 3-bromobenzenethiol with 2-bromoethanol according to the method used in Example 18, gave 2-(3-bromophenylthio)ethanol (125) as a yellow oil without purification. Yield (3.6 g, 97%): 1H NMR (400 MHz, CDCl3) δ 7.49 (t, J=2.0 Hz, 1H), 7.31 (ddd, J=0.8, 1.6, 8.0 Hz, 1H), 7.27 (ddd, J=0.8, 1.6, 8.0 Hz, 1H), 7.13 (t, J=7.6 Hz, 1H), 3.75 (t, J=6.4 Hz, 2H), 3.10 (t, J=6.4 Hz, 2H), 2.18 (brs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492589B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-aeeed436d4db44769e20825af984f736 |
| Source note | uspto-grants-2013_07 |