HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016183Generated: October 25, 2026
3-(Methoxycarbonyl)benzoic acid → Benzoic acid, 3-(hydroxymethyl)-, methyl ester
https://huagongshe.com/reaction/1016183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Methoxycarbonyl)benzoic acid | HCID 601880 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzoic acid, 3-(hydroxymethyl)-, methyl ester | HCID 155058 | 87.3% |
Reaction Steps
A solution of 3-(methoxycarbonyl)benzoic acid (1.05 g, 5.83 mmol) in THF (25 mL) was cooled to 0° C., and treated with the dropwise addition of 2.0 M borane-methylsulfide complex in THF (14.57 mL, 29.1 mmol) at a rate which did not allow the temperature to exceed 5° C. The mixture was stirred at 0° C. for 15 minutes, then allowed to warm to room temperature and stirred for 4 hours. The reaction was cooled to 0° C. and quenched with the addition of small pieces of ice, causing vigorous gas evolution. When gas evolution had ceased, the mixture was diluted with brine and extracted 3× with ethyl acetate. The combined organic phases were washed 3× with dilute bleach to remove residual methyl sulfide, 3× with saturated sodium carbonate to remove any unreacted acid, 1× with water, and 1× with brine, then dried over sodium sulfate and concentrated in vacuo to yield the title compound (845 mg, 5.09 mmol, 87% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07985861B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-f8290a5193d64234a1f4224c4318362f |
|---|
| Source note | uspto-grants-2011_07 |
|---|