HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Phosphorus tribromide → HCID 86715431, compound

HRID 1503648
Notes
Print preview

Reaction equation

HRID 1503648 reaction equation
[F:1][C:2]1[CH:14]=[C:13]([CH2:15]O)[CH:12]=[C:11]([O:17][CH3:18])[C:3]=1[O:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7].P(Br)(Br)[Br:20]>ClCCl>[Br:20][CH2:15][C:13]1[CH:12]=[C:11]([O:17][CH3:18])[C:3]([O:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])=[C:2]([F:1])[CH:14]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24614Phosphorus tribromideHCID 71014608HCID 71014608, compound

Product 1

HCID 86715431HCID 86715431, compoundYield 54%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The compound was prepared according to general procedure G with ethyl 2-(2-fluoro-4-(hydroxymethyl)-6-methoxyphenoxy)acetate (0.4 mmol) in dichloromethane (5 ml) and PBr3 (0.4 mmol). 67 mg of compound were obtained (54% yield). This compound was used without further purification. 1H NMR (250 MHz, CDCl3): δ 1.29 (t, J=7.0 Hz, 3H), 3.89 (s, 3H), 4.25 (q, J=7.0 Hz, 2H), 4.41 (s, 2H), 4.71 (s, 2H) 6.74 (m, 1H), 6.81 (m, 1H). MS (ESI): m/z 319.9 [M+H]+

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-2f1d1ab433f84605be544d1ca15dda6f
Source dataset
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09212196B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes