HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 22237497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 69627749 | HCID 69627749 | — |
| Product | HCID 22237497 | HCID 22237497 | — |
Reaction Steps
The title compound was prepared as an off white solid (0.167 g, 85%) from (5′-butoxy-[1,1′;3′1″]terphenyl-2′-yloxy)acetic acid methyl ester using a procedure similar to step 2 of Example 36, mp 92-94° C.; 1H NMR (DMSO-d6) δ0.92 (t, J=7.5 Hz, 3H), 1.38-1.49 (m, 2H), 1.65-1.74 (m, 2H), 3.64 (s, 2H), 4.02 (t, J=6.6 Hz, 2H), 6.87 (s, 2H), 7.33-7.39 (m, 2H), 7.39-7.44 (m, 4H), 7.57-7.61 (m, 4H), 12.30-12.55 (bs, 1H); IR (KBr) 3420, 3060, 2930, 2860, 2770, 2590, 1725, 1590, 1570, 1460, 1420, 1360, 1260, 1235, 1215, 1195, 1075, 1050, 1010, 925, 760, 750, 700, and 620 cm−1; mass spectrum [(+) ESI], m/z 394 (M+NH4)+; Anal. Calcd. for C24H24O4: C, 76.57; H, 6.43; N, 0.00, Found: C, 76.33; H, 6.55; N, −0.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214877B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-b925a0db5e8b4f3282c4239f5d8a93d3 |
| Source note | uspto-grants-2001_04 |