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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32114Generated: October 29, 2026

Tert-butyl 6-formyl-1,2,3,4-tetrahydronaphthalen-1-ylcarbamate → Tert-butyl 6-(1-hydroxyethyl)-1,2,3,4-tetrahydronaphthalen-1-ylcarbamate

https://huagongshe.com/reaction/32114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 6-formyl-1,2,3,4-tetrahydronaphthalen-1-ylcarbamateHCID 58841363—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 6-(1-hydroxyethyl)-1,2,3,4-tetrahydronaphthalen-1-ylcarbamateHCID 68681678—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (6-formyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-carbamic acid tert-butyl ester (Step c, 2.80 g, 10.2 mmol, 1.0 eq) in THF (100 mL) at −78° C. was added a solution of MeMgBr (Aldrich, 1.4 M in toluene/THF (3:1), 29 mL, 40.7 mmol, 4.0 eq) slowly. The reaction was stirred at −78° C. for 20 min, warmed to RT and stirred at RT for 2 h. The reaction was quenched with saturated NaHCO3 (120 mL), and the crude was extracted with EtOAc (100 mL×3). The extract phase was washed with saturated NaCl, dried over Na2SO4, filtered and concentrated. The title compound was obtained as a white solid. MS (ESI, pos. ion) m/z: 292 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425631B2
Source datasetuspto-grants-2008_09
ORD IDord-662ccd5a5fa843af9d54d6491a773466
Source noteuspto-grants-2008_09