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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243780Generated: October 30, 2026

Sodium borohydride → HCID 21064711, compound

https://huagongshe.com/reaction/1243780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21064712HCID 21064712—
SolventMethanolHCID 887—
ProductHCID 21064711HCID 2106471199.5%

Reaction Steps

6-(2-tert-Butoxycarbonylamino-acetyl)-nicotinic acid methyl ester (132.7 mg, 0.451 mmol) was dissolved into 3 mL of MeOH. To this was added sodium borohydride (18.96 mg, 0.50 mmol) in one portion. After 0.5 h, the reaction mixture was concentrated on a rotary evaporator. The residue was dissolved into 20 mL of EtOAc. The organic phase was washed with 2×20 mL NH4Cl and 1×20 mL of brine, dried (MgSO4) filtered and concentrated to give 133 mg, 99.5% of 6-(2-tert-butoxycarbonylamino-1-hydroxy-ethyl)-nicotinic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119102B2
Source datasetuspto-grants-2006_10
ORD IDord-6d4818735b744cb68167d936f55ff984
Source noteuspto-grants-2006_10