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

Trimethyl borate → 2-Fluoro-3-iodobenzyl alcohol

HRID 2096972
Notes
Print preview

Reaction equation

HRID 2096972 reaction equation
B(OC)(OC)OC.[F:8][C:9]1[C:17]([I:18])=[CH:16][CH:15]=[CH:14][C:10]=1[C:11](O)=[O:12]>O1CCCC1>[F:8][C:9]1[C:17]([I:18])=[CH:16][CH:15]=[CH:14][C:10]=1[CH2:11][OH:12]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 8470Trimethyl borateHCID 110545892-Fluoro-3-iodobenzoic acid

Product 1

HCID 120412982-Fluoro-3-iodobenzyl alcoholYield 97%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

Trimethyl borate (1.92 mL, 17.2 mmol) was added dropwise to a stirred solution of 2-fluoro-3-iodobenzoic acid (preparation 22b, 4.39 g, 16.5 mmol) in tetrahydrofuran (25 mL) at 0° C. and the mixture was stirred for a further 15 minutes at this temperature. Then borane-methyl sulfide complex (10 M, 4.4 mL, 44 mmol) in tetrahydrofuran (3 mL) was added dropwise to the mixture at 0° C. and the mixture was then allowed to warm to room temperature. After 1 hour, the mixture was carefully quenched by dropwise addition of methanol (10 mL). After stirring overnight, the mixture was concentrated in vacuo and ethyl acetate was added to the residue. The organic layer was washed with saturated aqueous potassium carbonate solution, brine, dried (MgSO4) and evaporated to give the title compound (4.03 g, 97%) as an oil.

Workup

  1. waitAfter 1 hour
  2. customthe mixture was carefully quenched by dropwise addition of methanol (10 mL)
  3. stirringAfter stirring overnight
  4. concentrationthe mixture was concentrated in vacuo and ethyl acetate
  5. additionwas added to the residue
  6. washThe organic layer was washed with saturated aqueous potassium carbonate solution, brine
  7. dry with materialdried (MgSO4)
  8. customevaporated

Sources & evidence

ORD record
ord-a3299156cbdd4da2b0436335fbd7808c
Source dataset
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08450341B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes