HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433097Generated: October 31, 2026
Carbon tetrabromide → HCID 69027125, compound
https://huagongshe.com/reaction/1433097
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 69026499 | HCID 69026499 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69027125 | HCID 69027125 | — |
Reaction Steps
(6′-methoxy-3,4,5,6-tetrahydro-2H-[1,3′]bipyridinyl-4-yl)-methanol (300 mg, 1.35 mmol) is dissolved in methylene chloride (10 mL). carbon tetrabromide (561 mg, 1.69 mmol) is added and dissolved. The solution is cooled to 0° C. and triphenylphoshine (529 mg, 2.02 mmol) is added portionwise. The reaction is allowed to come to r.t. and is stirred for 30 min. The volume is then reduced under vacuum to ˜2 ml and purified by flash chromatography on silica gel using 2% methanol/methylene chloride as the eluent to provide 4-bromomethyl-6′-methoxy-3,4,5,6-tetrahydro-2H-[1,3′]bipyridinyl. 1H NMR (300 MHz, CD3OD) δ 7.74 (d, 1H), 7.43 (dd, 1H), 6.72 (d, 1H), 3.83 (s, 3H), 3.54 (m, 2H), 3.38 (d, 2H), 2.65 (dt, 2H), 1.94 (m, 2H), 1.75 (m, 1H), 1.44 (m, 2H); MS (EI) 284 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-73b16ee9db064530867430a2889463bc |
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| Source note | uspto-grants-2009_11 |
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