HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718072Generated: October 29, 2026
Hydrochloric Acid → N-Boc-trans-4-hydroxy-L-prolinol
https://huagongshe.com/reaction/718072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | (2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester | HCID 2734883 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Boc-trans-4-hydroxy-L-prolinol | HCID 11275979 | 95.3% |
Reaction Steps
To a solution of compound 236 (6.4 g, 26.09 mmol) in THF (80 mL) at 0° C. was added a solution of LiBH4 (2.063 g, 94.76 mmol) in one shot. The suspension was stirred at 0° C. for 1 h then at room temperature overnight. The mixture was cooled to 0° C. and water (52 mL) then 6N HCl (20 mL) were added. The layers were separated and the aqueous layer was extracted with ethyl acetate (3×70 mL). The combined organics were washed with 2N NaOH, 2N HCl and brine (20 mL each). The organic layers were dried over Na2SO4 filtered and concentrated to afford title compound 237 (5.4 g, 95%) as clear oil. LRMS (ESI): (calc.) 217.13. (found) 256.3 (M+K).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09193749B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-37ac790ffed7474fad539b627ee9429c |
|---|
| Source note | uspto-grants-2015_11 |
|---|