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

Triethylamine → methyl (5-(3-hydroxyphenyl)-2H-tetrazol-2-yl)acetate

HRID 1960116
Notes
Print preview

Reaction equation

HRID 1960116 reaction equation
[N:1]1[NH:2][N:3]=[N:4][C:5]=1[C:6]1[CH:7]=[C:8]([OH:12])[CH:9]=[CH:10][CH:11]=1.CCN(CC)CC.Br[CH2:21][C:22]([O:24][CH3:25])=[O:23]>CC#N>[OH:12][C:8]1[CH:7]=[C:6]([C:5]2[N:4]=[N:3][N:2]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:1]=2)[CH:11]=[CH:10][CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 60984Methyl bromoacetateHCID 134557633-(2H-Tetrazol-5-yl)phenol

Product 1

HCID 58482535methyl (5-(3-hydroxyphenyl)-2H-tetrazol-2-yl)acetate

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

To a solution of 3-(2H-tetrazol-5-yl)phenol (250.8 mg, 1.547 mmol) in MeCN (10 mL) at rt was added Et3N (0.237 mL, 1.701 mmol) followed by methyl bromoacetate (260 mg, 1.701 mmol). The reaction was stirred at rt for 16 h. Volatiles were removed. Chromatography over silica eluting with 30-60% EtOAc/hexanes afforded the title compound as a white solid. 1H NMR (500 MHz, CDC13): δ 7.75 (d, 1H, J=7.5 Hz), 7.69 (s, 1H), 7.39 (t, 1H, J=8.0 Hz), 7.01 (dd, 1H, J=8.0, 2.3 Hz), 5.53 (bs, 1H), 5.50 (s, 2H), 3.86 (s, 3H).

Workup

  1. customVolatiles were removed

Sources & evidence

ORD record
ord-7899edaf04a74921b7648ee3d4e54ae6
Source dataset
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08410284B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes